Linked Data
ClinVar Variation Id:
566030
ClinVar RCV Id:
RCV000685741
dbSNP Id:
rs763954095
ExAC:
7:128483620 G / A
gnomAD v2:
7-128483620-G-A
gnomAD v3:
7-128843566-G-A
gnomAD v4:
7-128843566-G-A
COSMIC:
COSM1447945
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128843566G>A , CM000669.2:g.128843566G>A | GRCh38 |
| NC_000007.13:g.128483620G>A , CM000669.1:g.128483620G>A | GRCh37 |
| NC_000007.12:g.128270856G>A | NCBI36 |
| NG_011807.1:g.18138G>A , LRG_870:g.18138G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000325888.13:c.2800G>A MANE Select | ENSP00000327145.8:p.Ala934Thr | |
| ENST00000325888.12:c.2800G>A | ENSP00000327145.8:p.Ala934Thr | |
| ENST00000346177.6:c.2800G>A | ENSP00000344002.6:p.Ala934Thr | |
| NM_001127487.1:c.2800G>A | NP_001120959.1:p.Ala934Thr | |
| NM_001458.4:c.2800G>A , LRG_870t1:c.2800G>A | NP_001449.3:p.Ala934Thr | |
| NM_001127487.2:c.2800G>A | NP_001120959.1:p.Ala934Thr | |
| NM_001458.5:c.2800G>A MANE Select | NP_001449.3:p.Ala934Thr |