Linked Data
ClinVar Variation Id:
323363
ClinVar RCV Id:
RCV000277431
dbSNP Id:
rs774448424
ExAC:
17:41063291 G / A
gnomAD v2:
17-41063291-G-A
gnomAD v3:
17-42911274-G-A
gnomAD v4:
17-42911274-G-A
COSMIC:
COSM1610291
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42911274G>A , CM000679.2:g.42911274G>A | GRCh38 |
| NC_000017.10:g.41063291G>A , CM000679.1:g.41063291G>A | GRCh37 |
| NC_000017.9:g.38316817G>A | NCBI36 |
| NG_011808.1:g.15477G>A , LRG_147:g.15477G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253801.7:c.922G>A MANE Select | ENSP00000253801.1:p.Val308Ile | |
| ENST00000253801.6:c.922G>A | ENSP00000253801.1:p.Val308Ile | |
| ENST00000585489.1:c.*314G>A | ENSP00000466202.1:n.*314G>A | |
| ENST00000592383.5:c.*314G>A | ENSP00000465958.1:n.*314G>A | |
| NM_000151.3:c.922G>A | NP_000142.2:p.Val308Ile | |
| NM_001270397.1:c.*314G>A | NP_001257326.1:n.*314G>A | |
| NM_000151.4:c.922G>A MANE Select | NP_000142.2:p.Val308Ile | |
| NM_001270397.2:c.*314G>A | NP_001257326.1:n.*314G>A |