Linked Data
dbSNP Id:
rs959153278
gnomAD v2:
3-186566781-C-T
gnomAD v3:
3-186848992-C-T
gnomAD v4:
3-186848992-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.186848992C>T , CM000665.2:g.186848992C>T | GRCh38 |
| NC_000003.11:g.186566781C>T , CM000665.1:g.186566781C>T | GRCh37 |
| NC_000003.10:g.188049475C>T | NCBI36 |
| NG_021140.1:g.11319C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000320741.7:c.-8-4059C>T MANE Select | ENSP00000320709.2:n.-8-4059C>T | |
| ENST00000320741.6:c.-8-4059C>T | ENSP00000320709.2:n.-8-4059C>T | |
| ENST00000444204.2:c.-9+3385C>T | ENSP00000389814.2:n.-9+3385C>T | |
| NM_001177800.1:c.-9+3385C>T | NP_001171271.1:n.-9+3385C>T | |
| NM_004797.3:c.-8-4059C>T | NP_004788.1:n.-8-4059C>T | |
| XM_011513324.1:c.-124-2114C>T | XP_011511626.1:n.-124-2114C>T | |
| NM_004797.4:c.-8-4059C>T MANE Select | NP_004788.1:n.-8-4059C>T | |
| NM_001177800.2:c.-9+3385C>T | NP_001171271.1:n.-9+3385C>T |