Linked Data
ClinVar Variation Id:
297576
ClinVar RCV Id:
RCV000402493
dbSNP Id:
rs574908976
gnomAD v2:
1-52838759-G-A
gnomAD v3:
1-52373087-G-A
gnomAD v4:
1-52373087-G-A
COSMIC:
COSN24389753
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.52373087G>A , CM000663.2:g.52373087G>A | GRCh38 |
| NC_000001.10:g.52838759G>A , CM000663.1:g.52838759G>A | GRCh37 |
| NC_000001.9:g.52611347G>A | NCBI36 |
| NG_028251.1:g.36385C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371568.8:c.*94C>T MANE Select | ENSP00000360623.3:n.*94C>T | |
| ENST00000371566.1:c.*94C>T | ENSP00000360621.1:n.*94C>T | |
| ENST00000371568.7:c.*94C>T | ENSP00000360623.3:n.*94C>T | |
| NM_001190818.1:c.*94C>T | NP_001177747.1:n.*94C>T | |
| NM_001190819.1:c.*94C>T | NP_001177748.1:n.*94C>T | |
| NM_004153.3:c.*94C>T | NP_004144.2:n.*94C>T | |
| XM_011541527.1:c.*94C>T | XP_011539829.1:n.*94C>T | |
| XM_011541527.3:c.*94C>T | XP_011539829.1:n.*94C>T | |
| XM_017001388.2:c.*94C>T | XP_016856877.1:n.*94C>T | |
| XM_017001389.2:c.*94C>T | XP_016856878.1:n.*94C>T | |
| NM_004153.4:c.*94C>T MANE Select | NP_004144.2:n.*94C>T | |
| NM_001190818.2:c.*94C>T | NP_001177747.1:n.*94C>T | |
| NM_001190819.2:c.*94C>T | NP_001177748.1:n.*94C>T |