Linked Data
dbSNP Id:
rs188913899
gnomAD v2:
3-121769363-C-A
gnomAD v3:
3-122050516-C-A
gnomAD v4:
3-122050516-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.122050516C>A , CM000665.2:g.122050516C>A | GRCh38 |
| NC_000003.11:g.121769363C>A , CM000665.1:g.121769363C>A | GRCh37 |
| NC_000003.10:g.123252053C>A | NCBI36 |
| NG_029928.1:g.155C>A | |
| NG_031870.2:g.15039G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011512739.1:c.-348+9904G>T | XP_011511041.1:n.-348+9904G>T | |
| XM_011512739.2:c.-348+9904G>T | XP_011511041.1:n.-348+9904G>T |