Linked Data
ClinVar Variation Id:
1764595
ClinVar RCV Id:
RCV002373612
dbSNP Id:
rs538010963
gnomAD v3:
5-173232668-G-A
gnomAD v4:
5-173232668-G-A
COSMIC:
COSM295285
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.173232668G>A , CM000667.2:g.173232668G>A | GRCh38 |
| NC_000005.9:g.172659671G>A , CM000667.1:g.172659671G>A | GRCh37 |
| NC_000005.8:g.172592277G>A | NCBI36 |
| NG_013340.1:g.7645C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000329198.5:c.876C>T MANE Select | ENSP00000327758.4:p.Phe292= | |
| ENST00000329198.4:c.876C>T | ENSP00000327758.4:p.Phe292= | |
| NM_001166175.1:c.*829C>T | NP_001159647.1:n.*829C>T | |
| NM_001166176.1:c.*675C>T | NP_001159648.1:n.*675C>T | |
| NM_004387.3:c.876C>T | NP_004378.1:p.Phe292= | |
| NM_004387.4:c.876C>T MANE Select | NP_004378.1:p.Phe292= | |
| NM_001166175.2:c.*829C>T | NP_001159647.1:n.*829C>T | |
| NM_001166176.2:c.*675C>T | NP_001159648.1:n.*675C>T |