dbSNP:
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.85292513 (EAS)
Genomes Max Group AF
0.85292513 (EAS)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.86696058A>G , CM000669.2:g.86696058A>G | GRCh38 |
| NC_000007.13:g.86325374A>G , CM000669.1:g.86325374A>G | GRCh37 |
| NC_000007.12:g.86163310A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361669.7:c.-141+51186A>G MANE Select | ENSP00000355316.2:n.-141+51186A>G | |
| ENST00000361669.6:c.-141+51186A>G | ENSP00000355316.2:n.-141+51186A>G | |
| ENST00000421579.1:c.-141+51087A>G | ENSP00000390037.1:n.-141+51087A>G | |
| ENST00000439827.1:c.-141+51186A>G | ENSP00000398767.1:n.-141+51186A>G | |
| ENST00000454217.1:c.84+51186A>G | ENSP00000405427.1:n.84+51186A>G | |
| NM_000840.2:c.-141+51186A>G | NP_000831.2:n.-141+51186A>G | |
| XM_011516088.1:c.-141+51186A>G | XP_011514390.1:n.-141+51186A>G | |
| XM_011516089.1:c.-141+51186A>G | XP_011514391.1:n.-141+51186A>G | |
| XM_011516090.1:c.-141+51186A>G | XP_011514392.1:n.-141+51186A>G | |
| NM_001363522.1:c.-141+51186A>G | NP_001350451.1:n.-141+51186A>G | |
| XM_017012073.2:c.-141+51186A>G | XP_016867562.1:n.-141+51186A>G | |
| NM_000840.3:c.-141+51186A>G MANE Select | NP_000831.2:n.-141+51186A>G | |
| NM_001363522.2:c.-141+51186A>G | NP_001350451.1:n.-141+51186A>G |