Linked Data
ClinVar Variation Id:
382485
dbSNP Id:
rs764850069
ExAC:
9:127245226 G / A
gnomAD v2:
9-127245226-G-A
gnomAD v3:
9-124482947-G-A
gnomAD v4:
9-124482947-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.124482947G>A , CM000671.2:g.124482947G>A | GRCh38 |
| NC_000009.11:g.127245226G>A , CM000671.1:g.127245226G>A | GRCh37 |
| NC_000009.10:g.126285047G>A | NCBI36 |
| NG_008176.1:g.29474C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373588.9:c.1197C>T MANE Select | ENSP00000362690.4:p.Ala399= | |
| ENST00000373587.3:c.549C>T | ENSP00000362689.3:p.Ala183= | |
| ENST00000373588.8:c.1197C>T | ENSP00000362690.4:p.Ala399= | |
| ENST00000620110.4:c.1077C>T | ENSP00000483309.1:p.Ala359= | |
| NM_004959.4:c.1197C>T | NP_004950.2:p.Ala399= | |
| XM_005251871.2:c.1197C>T | XP_005251928.1:p.Ala399= | |
| XM_005251872.3:c.936C>T | XP_005251929.1:p.Ala312= | |
| XM_011518455.1:c.1197C>T | XP_011516757.1:p.Ala399= | |
| XM_011518456.1:c.*53C>T | XP_011516758.1:n.*53C>T | |
| NM_004959.5:c.1197C>T MANE Select | NP_004950.2:p.Ala399= |