The GOATs- best teams and players from various generations. The players are ranked within the generation they played. Presenting the rankings for 5 generations starting from oldest to newest. For the last update date and full update schedule, refer to FAQs.
Gen1
Gen2
Gen3
Gen4
Gen5
| Group | Sub-Group | SG_rank | Team (or Player) | Stats |
|---|---|---|---|---|
| World_100 | Gen1 | 1 |
|
1948-1958 | M-11 | R-862 | A-57 | SR*-53 | avgCR-44.57 | CI*- 28 22 na na 36 25 31 7 |
| World_100 | Gen1 | 2 |
|
1934-1951 | M-14 | R-1007 | A-42 | SR*-35 | avgCR-39.27 | CI*- 21 20 na na 21 32 13 14 |
| World_100 | Gen1 | 3 |
|
1934-1954 | M-15 | R-872 | A-36 | SR*-42 | avgCR-34.85 | CI*- 16 21 na na 17 20 27 12 |
| World_100 | Gen1 | 4 |
|
1934-1949 | M-10 | R-613 | A-41 | SR*-40 | avgCR-36.75 | CI*- 17 20 na na 4 28 28 12 |
| World_100 | Gen1 | 5 |
|
1949-1963 | M-14 | R-829 | A-33 | SR*-24 | avgCR-29.59 | CI*- 11 18 na na 15 22 15 7 |
| World_100 | Gen1 | 6 |
|
1949-1963 | M-17 | R-652 | A-24 | SR*-38 | avgCR-22.98 | CI*- 11 14 na na 12 14 14 7 |
| World_100 | Gen1 | 7 |
|
1957-1961 | M-5 | R-296 | A-37 | SR*-37 | avgCR-34.86 | CI*- na 19 na na 5 38 23 18 |
| World_100 | Gen1 | 8 |
|
1934-1937 | M-6 | R-340 | A-28 | SR*-34 | avgCR-35.14 | CI*- 5 30 na na 18 22 17 13 |
| World_100 | Gen1 | 9 |
|
1957-1963 | M-11 | R-476 | A-32 | SR*-36 | avgCR-24.70 | CI*- 7 17 na na 17 16 12 8 |
| World_100 | Gen1 | 10 |
|
1934-1937 | M-6 | R-335 | A-28 | SR*-30 | avgCR-31.40 | CI*- 11 21 na na 22 19 13 5 |
| World_100 | Gen1 | 11 |
|
1935-1951 | M-9 | R-451 | A-35 | SR*-27 | avgCR-25.11 | CI*- 15 14 na na 11 15 19 12 |
| World_100 | Gen1 | 12 |
|
1960-1961 | M-4 | R-240 | A-34 | SR*-46 | avgCR-34.00 | CI*- 17 na na na 39 13 9 5 |
| World_100 | Gen1 | 13 |
|
1960-1961 | M-4 | R-226 | A-45 | SR*-37 | avgCR-29.85 | CI*- na 17 na na 31 10 4 16 |
| World_100 | Gen1 | 14 |
|
1948-1961 | M-12 | R-471 | A-28 | SR*-32 | avgCR-18.38 | CI*- 11 9 na na 24 8 4 3 |
| World_100 | Gen1 | 15 |
|
1951-1954 | M-6 | R-288 | A-32 | SR*-43 | avgCR-26.41 | CI*- 14 na na na 15 27 12 10 |
| World_100 | Gen1 | 16 |
|
1949-1958 | M-13 | R-436 | A-20 | SR*-33 | avgCR-19.85 | CI*- 14 9 na na 16 5 9 11 |
| World_100 | Gen1 | 17 |
|
1951-1958 | M-8 | R-286 | A-24 | SR*-39 | avgCR-23.08 | CI*- 13 12 na na 14 8 19 5 |
| World_100 | Gen1 | 18 |
|
1949-1961 | M-8 | R-255 | A-26 | SR*-43 | avgCR-16.56 | CI*- 8 15 na na 17 13 1 3 |
| World_100 | Gen1 | 19 |
|
1948-1966 | M-12 | R-371 | A-18 | SR*-26 | avgCR-17.87 | CI*- 6 12 na na 12 10 7 8 |
| World_100 | Gen2 | 1 |
|
1960-1979 | M-22 | R-1594 | A-46 | SR*-35 | avgCR-32.00 | CI*- 18 16 na na 20 20 18 9 |
| World_100 | Gen2 | 2 |
|
1968-1979 | M-12 | R-1078 | A-60 | SR*-41 | avgCR-41.27 | CI*- 22 23 na na 23 20 26 20 |
| World_100 | Gen2 | 3 |
|
1966-1975 | M-11 | R-779 | A-43 | SR*-31 | avgCR-34.28 | CI*- 20 16 na na 12 22 12 29 |
| World_100 | Gen2 | 4 |
|
1975-1977 | M-7 | R-499 | A-62 | SR*-39 | avgCR-32.24 | CI*- 30 18 na na 14 24 27 13 |
| World_100 | Gen2 | 5 |
|
1975-1979 | M-5 | R-400 | A-44 | SR*-30 | avgCR-39.44 | CI*- 27 15 na na 8 19 36 5 |
| World_100 | Gen2 | 6 |
|
1976-1979 | M-11 | R-472 | A-28 | SR*-37 | avgCR-24.94 | CI*- 14 16 na na 15 11 13 51 |
| World_100 | Gen2 | 7 |
|
1966-1976 | M-10 | R-610 | A-41 | SR*-34 | avgCR-27.22 | CI*- 19 12 na na 21 13 15 11 |
| World_100 | Gen2 | 8 |
|
1976-1977 | M-6 | R-345 | A-43 | SR*-41 | avgCR-24.11 | CI*- 2 20 na na 14 25 2 15 |
| World_100 | Gen2 | 9 |
|
1966-1979 | M-15 | R-699 | A-29 | SR*-30 | avgCR-19.68 | CI*- 13 8 na na 13 4 13 2 |
| World_100 | Gen2 | 10 |
|
1972-1972 | M-3 | R-184 | A-31 | SR*-24 | avgCR-36.09 | CI*- 18 na na na 4 18 5 32 |
| World_100 | Gen2 | 11 |
|
1966-1972 | M-9 | R-433 | A-27 | SR*-32 | avgCR-24.82 | CI*- 13 12 na na 19 4 17 7 |
| World_100 | Gen2 | 12 |
|
1968-1977 | M-5 | R-261 | A-37 | SR*-37 | avgCR-24.94 | CI*- 14 na na na 31 5 19 6 |
| World_100 | Gen2 | 13 |
|
1966-1969 | M-5 | R-212 | A-35 | SR*-26 | avgCR-24.60 | CI*- 5 17 na na 6 29 7 12 |
| World_100 | Gen2 | 14 |
|
1954-1966 | M-13 | R-378 | A-22 | SR*-38 | avgCR-18.26 | CI*- 3 13 na na 15 9 10 6 |
| World_100 | Gen2 | 15 |
|
1976-1979 | M-11 | R-324 | A-19 | SR*-38 | avgCR-18.70 | CI*- 6 13 na na 10 16 10 6 |
| World_100 | Gen2 | 16 |
|
1972-1977 | M-8 | R-341 | A-28 | SR*-39 | avgCR-20.19 | CI*- 11 13 na na 4 16 25 3 |
| World_100 | Gen2 | 17 |
|
1976-1979 | M-9 | R-348 | A-29 | SR*-37 | avgCR-19.72 | CI*- 21 10 na na 15 12 10 na |
| World_100 | Gen2 | 18 |
|
1976-1979 | M-11 | R-293 | A-21 | SR*-40 | avgCR-16.33 | CI*- 5 11 na na 11 11 8 5 |
| World_100 | Gen2 | 19 |
|
1957-1969 | M-15 | R-426 | A-25 | SR*-41 | avgCR-14.36 | CI*- 7 8 na na 12 8 5 5 |
| World_100 | Gen2 | 20 |
|
1957-1969 | M-10 | R-391 | A-24 | SR*-35 | avgCR-18.37 | CI*- 17 9 na na 8 7 13 16 |
| World_100 | Gen2 | 21 |
|
1968-1985 | M-13 | R-397 | A-18 | SR*-36 | avgCR-16.75 | CI*- 11 8 na na 6 7 14 10 |
| World_100 | Gen3 | 1 |
|
1979-1998 | M-27 | R-1935 | A-50 | SR*-35 | avgCR-32.81 | CI*- 18 19 na na 22 19 16 14 |
| World_100 | Gen3 | 2 |
|
1979-1996 | M-19 | R-1301 | A-52 | SR*-30 | avgCR-31.49 | CI*- 21 19 na na 22 26 9 24 |
| World_100 | Gen3 | 3 |
|
1987-1992 | M-10 | R-819 | A-82 | SR*-38 | avgCR-34.53 | CI*- 19 24 na na 17 39 14 2 |
| World_100 | Gen3 | 4 |
|
1984-1995 | M-13 | R-1110 | A-50 | SR*-31 | avgCR-38.64 | CI*- 25 18 na na 21 36 16 13 |
| World_100 | Gen3 | 5 |
|
1984-1992 | M-18 | R-1164 | A-40 | SR*-33 | avgCR-32.53 | CI*- 22 16 na na 16 15 24 23 |
| World_100 | Gen3 | 6 |
|
1987-1992 | M-10 | R-762 | A-59 | SR*-37 | avgCR-33.09 | CI*- 21 21 na na 16 32 19 6 |
| World_100 | Gen3 | 7 |
|
1986-1986 | M-3 | R-290 | A-48 | SR*-42 | avgCR-53.29 | CI*- 27 na na na 4 34 5 41 |
| World_100 | Gen3 | 8 |
|
1977-1985 | M-13 | R-765 | A-40 | SR*-37 | avgCR-28.56 | CI*- 12 27 na na 20 22 16 6 |
| World_100 | Gen3 | 9 |
|
1979-1985 | M-12 | R-702 | A-37 | SR*-41 | avgCR-27.07 | CI*- 14 20 na na 6 22 4 19 |
| World_100 | Gen3 | 10 |
|
1976-1991 | M-16 | R-750 | A-33 | SR*-28 | avgCR-23.76 | CI*- 13 11 na na 14 19 4 11 |
| World_100 | Gen3 | 11 |
|
1984-1987 | M-10 | R-510 | A-39 | SR*-38 | avgCR-26.33 | CI*- 12 19 na na 14 21 21 4 |
| World_100 | Gen3 | 12 |
|
1969-1985 | M-7 | R-465 | A-36 | SR*-32 | avgCR-34.85 | CI*- 27 16 na na 13 12 29 18 |
| World_100 | Gen3 | 13 |
|
1984-1987 | M-7 | R-454 | A-41 | SR*-34 | avgCR-27.95 | CI*- 21 5 na na 25 24 8 6 |
| World_100 | Gen3 | 14 |
|
1984-1991 | M-12 | R-614 | A-28 | SR*-33 | avgCR-23.95 | CI*- 12 14 na na 10 7 18 8 |
| World_100 | Gen3 | 15 |
|
1987-1992 | M-7 | R-289 | A-29 | SR*-30 | avgCR-23.21 | CI*- 15 15 na na 21 16 9 5 |
| World_100 | Gen3 | 16 |
|
1984-1992 | M-15 | R-410 | A-41 | SR*-35 | avgCR-12.80 | CI*- 7 8 na na 14 10 2 1 |
| World_100 | Gen3 | 17 |
|
1976-1991 | M-19 | R-700 | A-23 | SR*-31 | avgCR-16.57 | CI*- 7 12 na na 17 7 5 4 |
| World_100 | Gen3 | 18 |
|
1976-1985 | M-13 | R-490 | A-23 | SR*-34 | avgCR-18.84 | CI*- 7 15 na na 13 7 14 4 |
| World_100 | Gen3 | 19 |
|
1976-1987 | M-17 | R-577 | A-21 | SR*-37 | avgCR-17.07 | CI*- 8 11 na na 7 12 9 8 |
| World_100 | Gen3 | 20 |
|
1976-1991 | M-21 | R-601 | A-19 | SR*-30 | avgCR-13.79 | CI*- 6 8 na na 8 5 10 5 |
| World_100 | Gen4 | 1 |
|
1995-2009 | M-14 | R-1002 | A-56 | SR*-56 | avgCR-38.79 | CI*- 11 30 na na 20 35 23 14 |
| World_100 | Gen4 | 2 |
|
1991-2005 | M-15 | R-919 | A-46 | SR*-45 | avgCR-30.89 | CI*- 14 22 na na 16 21 8 28 |
| World_100 | Gen4 | 3 |
|
1992-1996 | M-5 | R-433 | A-144 | SR*-52 | avgCR-36.20 | CI*- 21 32 na na 28 9 43 na |
| World_100 | Gen4 | 4 |
|
1998-2004 | M-3 | R-360 | A-60 | SR*-43 | avgCR-46.02 | CI*- 33 18 na na 33 50 8 7 |
| World_100 | Gen4 | 5 |
|
1990-1998 | M-10 | R-437 | A-109 | SR*-39 | avgCR-16.70 | CI*- 2 14 na na 8 19 11 0 |
| World_100 | Gen4 | 6 |
|
1999-2006 | M-7 | R-503 | A-50 | SR*-40 | avgCR-27.63 | CI*- 30 15 na na 13 29 na 6 |
| World_100 | Gen4 | 7 |
|
1995-1996 | M-6 | R-473 | A-68 | SR*-39 | avgCR-24.56 | CI*- 12 22 na na 26 28 6 na |
| World_100 | Gen4 | 8 |
|
2002-2003 | M-3 | R-239 | A-40 | SR*-35 | avgCR-43.70 | CI*- 20 23 na na 6 3 38 na |
| World_100 | Gen4 | 9 |
|
1995-1999 | M-5 | R-318 | A-35 | SR*-41 | avgCR-34.11 | CI*- 11 29 na na 23 12 19 26 |
| World_100 | Gen4 | 10 |
|
1995-1995 | M-4 | R-264 | A-53 | SR*-66 | avgCR-35.11 | CI*- 21 19 na na 18 29 16 15 |
| World_100 | Gen4 | 11 |
|
2001-2006 | M-4 | R-217 | A-43 | SR*-51 | avgCR-27.02 | CI*- 3 33 na na 4 34 na 2 |
| World_100 | Gen4 | 12 |
|
1995-1995 | M-3 | R-184 | A-61 | SR*-63 | avgCR-34.69 | CI*- 21 na na na 46 18 17 4 |
| World_100 | Gen4 | 13 |
|
1995-2006 | M-12 | R-548 | A-30 | SR*-32 | avgCR-21.05 | CI*- 12 13 na na 28 8 10 8 |
| World_100 | Gen4 | 14 |
|
1995-2005 | M-9 | R-378 | A-27 | SR*-37 | avgCR-22.88 | CI*- 3 16 na na 8 21 19 5 |
| World_100 | Gen4 | 15 |
|
1995-2003 | M-8 | R-441 | A-37 | SR*-33 | avgCR-23.42 | CI*- 15 13 na na 10 20 7 15 |
| World_100 | Gen4 | 16 |
|
1992-2006 | M-21 | R-554 | A-24 | SR*-31 | avgCR-12.84 | CI*- 7 8 na na 9 8 7 5 |
| World_100 | Gen4 | 17 |
|
1984-1996 | M-13 | R-365 | A-24 | SR*-27 | avgCR-14.00 | CI*- 10 8 na na 13 4 6 16 |
| World_100 | Gen4 | 18 |
|
1995-2003 | M-12 | R-436 | A-24 | SR*-37 | avgCR-15.76 | CI*- 10 6 na na 12 9 3 10 |
| World_100 | Gen4 | 19 |
|
1995-1998 | M-9 | R-441 | A-32 | SR*-38 | avgCR-18.40 | CI*- 12 8 na na 14 7 9 8 |
| World_100 | Gen4 | 20 |
|
1995-2005 | M-16 | R-502 | A-20 | SR*-34 | avgCR-13.26 | CI*- 8 6 na na 8 10 7 4 |
| World_100 | Gen5 | 1 |
|
1996-2015 | M-23 | R-1676 | A-44 | SR*-42 | avgCR-36.70 | CI*- 17 25 na na 15 18 26 20 |
| World_100 | Gen5 | 2 |
|
1999-2009 | M-15 | R-1030 | A-41 | SR*-44 | avgCR-33.38 | CI*- 19 16 na na 7 24 25 11 |
| World_100 | Gen5 | 3 |
|
2014-2024 | M-4 | R-395 | A-56 | SR*-60 | avgCR-56.71 | CI*- 20 31 na na 83 24 19 15 |
| World_100 | Gen5 | 4 |
|
2014-2024 | M-7 | R-629 | A-57 | SR*-64 | avgCR-42.10 | CI*- 21 24 na na 32 30 10 16 |
| World_100 | Gen5 | 5 |
|
2021-2025 | M-6 | R-586 | A-84 | SR*-62 | avgCR-39.49 | CI*- 24 24 na na 26 45 7 0 |
| World_100 | Gen5 | 6 |
|
2021-2024 | M-5 | R-567 | A-63 | SR*-74 | avgCR-48.93 | CI*- 21 30 na na 29 35 23 9 |
| World_100 | Gen5 | 7 |
|
2008-2025 | M-14 | R-930 | A-58 | SR*-46 | avgCR-29.24 | CI*- 16 16 na na 16 28 12 6 |
| World_100 | Gen5 | 8 |
|
2014-2025 | M-12 | R-883 | A-46 | SR*-55 | avgCR-31.21 | CI*- 17 18 na na 20 27 9 13 |
| World_100 | Gen5 | 9 |
|
2011-2025 | M-14 | R-970 | A-42 | SR*-48 | avgCR-29.91 | CI*- 12 20 na na 12 26 17 11 |
| World_100 | Gen5 | 10 |
|
2006-2014 | M-4 | R-331 | A-66 | SR*-55 | avgCR-42.35 | CI*- 15 31 na na 35 19 21 4 |
| World_100 | Gen5 | 11 |
|
2017-2025 | M-8 | R-559 | A-43 | SR*-53 | avgCR-32.78 | CI*- 19 22 na na 12 26 26 5 |
| World_100 | Gen5 | 12 |
|
2002-2021 | M-12 | R-699 | A-44 | SR*-45 | avgCR-26.74 | CI*- 16 16 na na 23 20 5 12 |
| World_100 | Gen5 | 13 |
|
2022-2024 | M-4 | R-299 | A-37 | SR*-43 | avgCR-43.73 | CI*- 12 25 na na 16 28 27 5 |
| World_100 | Gen5 | 14 |
|
2001-2014 | M-11 | R-551 | A-31 | SR*-32 | avgCR-27.05 | CI*- 12 18 na na 17 8 10 26 |
| World_100 | Gen5 | 15 |
|
2005-2011 | M-6 | R-295 | A-33 | SR*-36 | avgCR-32.75 | CI*- 8 26 na na 15 4 27 9 |
| World_100 | Gen5 | 16 |
|
2017-2025 | M-7 | R-358 | A-36 | SR*-50 | avgCR-25.13 | CI*- 8 29 na na 27 9 20 0 |
| World_100 | Gen5 | 17 |
|
2011-2025 | M-10 | R-489 | A-31 | SR*-57 | avgCR-24.06 | CI*- 14 14 na na 13 24 10 3 |
| World_100 | Gen5 | 18 |
|
2003-2011 | M-8 | R-416 | A-32 | SR*-36 | avgCR-28.52 | CI*- 19 10 na na 13 4 27 4 |
| World_100 | Gen5 | 19 |
|
2013-2025 | M-11 | R-612 | A-34 | SR*-49 | avgCR-22.01 | CI*- 13 13 na na 12 14 14 11 |
| World_100 | Gen5 | 20 |
|
2003-2017 | M-12 | R-444 | A-22 | SR*-31 | avgCR-19.52 | CI*- 10 12 na na 6 3 17 18 |