Linked Data
ClinVar Variation Id:
2602878
ClinVar RCV Id:
RCV003352150
dbSNP Id:
rs778090662
ExAC:
1:201286779 G / A
gnomAD v2:
1-201286779-G-A
gnomAD v3:
1-201317651-G-A
gnomAD v4:
1-201317651-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.201317651G>A , CM000663.2:g.201317651G>A | GRCh38 |
| NC_000001.10:g.201286779G>A , CM000663.1:g.201286779G>A | GRCh37 |
| NC_000001.9:g.199553402G>A | NCBI36 |
| NG_023337.1:g.39200G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367324.8:c.926G>A MANE Select | ENSP00000356293.4:p.Gly309Glu | |
| ENST00000263946.7:c.926G>A | ENSP00000263946.3:p.Gly309Glu | |
| ENST00000352845.3:c.926G>A | ENSP00000295597.3:p.Gly309Glu | |
| ENST00000367324.7:c.926G>A | ENSP00000356293.3:p.Gly309Glu | |
| ENST00000475988.1:n.268G>A | ||
| ENST00000622031.4:c.923G>A | ENSP00000482213.1:p.Gly308Glu | |
| NM_000299.3:c.926G>A | NP_000290.2:p.Gly309Glu | |
| NM_001005337.2:c.926G>A | NP_001005337.1:p.Gly309Glu | |
| NM_001005337.3:c.926G>A MANE Select | NP_001005337.1:p.Gly309Glu | |
| NM_000299.4:c.926G>A | NP_000290.2:p.Gly309Glu |