gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.66736392 (SAS)
Genomes Max Group AF
0.66736392 (SAS)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.68164294G>A , CM000673.2:g.68164294G>A | GRCh38 |
| NC_000011.9:g.67931761G>A , CM000673.1:g.67931761G>A | GRCh37 |
| NC_000011.8:g.67688337G>A | NCBI36 |
| NG_052873.1:g.54479C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453170.6:c.961+2688C>T | ENSP00000406377.2:n.961+2688C>T | |
| ENST00000524672.3:n.1526+2688C>T | ||
| ENST00000700520.1:c.*798+2688C>T | ENSP00000515027.1:n.*798+2688C>T | |
| ENST00000700521.1:c.*841+2688C>T | ENSP00000515028.1:n.*841+2688C>T | |
| ENST00000700522.1:c.*841+2688C>T | ENSP00000515029.1:n.*841+2688C>T | |
| ENST00000700523.1:c.658+2688C>T | ENSP00000515030.1:n.658+2688C>T | |
| ENST00000700524.1:c.*382+2688C>T | ENSP00000515031.1:n.*382+2688C>T | |
| ENST00000304363.9:c.1174+2688C>T MANE Select | ENSP00000305899.4:n.1174+2688C>T | |
| ENST00000304363.8:c.1174+2688C>T | ENSP00000305899.4:n.1174+2688C>T | |
| ENST00000427752.6:c.*762+2688C>T | ENSP00000387685.2:n.*762+2688C>T | |
| ENST00000441488.6:c.*382+2688C>T | ENSP00000411146.2:n.*382+2688C>T | |
| ENST00000615954.4:c.1174+2688C>T | ENSP00000484858.1:n.1174+2688C>T | |
| NM_001300907.1:c.658+2688C>T | NP_001287836.1:n.658+2688C>T | |
| NM_001300908.1:c.454+2688C>T | NP_001287837.1:n.454+2688C>T | |
| NM_017635.4:c.1174+2688C>T | NP_060105.3:n.1174+2688C>T | |
| XM_005274035.2:c.1174+2688C>T | XP_005274092.2:n.1174+2688C>T | |
| XM_005274036.2:c.1105+2688C>T | XP_005274093.2:n.1105+2688C>T | |
| XM_005274037.1:c.658+2688C>T | XP_005274094.1:n.658+2688C>T | |
| XM_006718581.1:c.1105+2688C>T | XP_006718644.1:n.1105+2688C>T | |
| XM_011545091.1:c.1174+2688C>T | XP_011543393.1:n.1174+2688C>T | |
| XM_011545092.1:c.961+2688C>T | XP_011543394.1:n.961+2688C>T | |
| XM_011545093.1:c.-69+2688C>T | XP_011543395.1:n.-69+2688C>T | |
| XM_005274035.4:c.1174+2688C>T | XP_005274092.2:n.1174+2688C>T | |
| XM_005274036.4:c.1105+2688C>T | XP_005274093.2:n.1105+2688C>T | |
| XM_006718581.2:c.1105+2688C>T | XP_006718644.1:n.1105+2688C>T | |
| XM_011545092.3:c.961+2688C>T | XP_011543394.1:n.961+2688C>T | |
| XM_017017876.2:c.658+2688C>T | XP_016873365.1:n.658+2688C>T | |
| XM_017017877.2:c.658+2688C>T | XP_016873366.1:n.658+2688C>T | |
| XM_017017878.2:c.658+2688C>T | XP_016873367.1:n.658+2688C>T | |
| XM_017017879.2:c.658+2688C>T | XP_016873368.1:n.658+2688C>T | |
| XM_024448570.1:c.-69+2688C>T | XP_024304338.1:n.-69+2688C>T | |
| NM_017635.5:c.1174+2688C>T MANE Select | NP_060105.3:n.1174+2688C>T | |
| NM_001300908.2:c.454+2688C>T | NP_001287837.1:n.454+2688C>T | |
| NM_001369426.1:c.1174+2688C>T | NP_001356355.1:n.1174+2688C>T | |
| NM_001369428.1:c.658+2688C>T | NP_001356357.1:n.658+2688C>T | |
| NM_001369429.1:c.658+2688C>T | NP_001356358.1:n.658+2688C>T | |
| NM_001369430.1:c.658+2688C>T | NP_001356359.1:n.658+2688C>T | |
| NM_001369431.1:c.658+2688C>T | NP_001356360.1:n.658+2688C>T | |
| NM_001369432.1:c.658+2688C>T | NP_001356361.1:n.658+2688C>T | |
| NM_001369433.1:c.658+2688C>T | NP_001356362.1:n.658+2688C>T |