Linked Data
ClinVar Variation Id:
293031
dbSNP Id:
rs561401543
ExAC:
1:158639333 G / A
gnomAD v2:
1-158639333-G-A
gnomAD v3:
1-158669543-G-A
gnomAD v4:
1-158669543-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.158669543G>A , CM000663.2:g.158669543G>A | GRCh38 |
| NC_000001.10:g.158639333G>A , CM000663.1:g.158639333G>A | GRCh37 |
| NC_000001.9:g.156905957G>A | NCBI36 |
| NG_011474.1:g.22174C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000643759.2:c.1698C>T MANE Select | ENSP00000495214.1:p.Ala566= | |
| ENST00000368147.8:c.1698C>T | ENSP00000357129.4:p.Ala566= | |
| ENST00000614909.4:c.1698C>T | ENSP00000482595.1:p.Ala566= | |
| NM_003126.2:c.1698C>T | NP_003117.2:p.Ala566= | |
| XM_011509916.1:c.1698C>T | XP_011508218.1:p.Ala566= | |
| XM_011509917.1:c.1698C>T | XP_011508219.1:p.Ala566= | |
| XM_011509918.1:c.1698C>T | XP_011508220.1:p.Ala566= | |
| XM_011509919.1:c.1698C>T | XP_011508221.1:p.Ala566= | |
| XR_921911.1:n.1811C>T | ||
| XR_921912.1:n.1816C>T | ||
| NM_003126.3:c.1698C>T | NP_003117.2:p.Ala566= | |
| XM_011509916.2:c.1698C>T | XP_011508218.1:p.Ala566= | |
| XM_011509917.3:c.1698C>T | XP_011508219.1:p.Ala566= | |
| XM_011509918.3:c.1698C>T | XP_011508220.1:p.Ala566= | |
| XM_011509919.3:c.1698C>T | XP_011508221.1:p.Ala566= | |
| XR_921911.3:n.1824C>T | ||
| XR_921912.2:n.1826C>T | ||
| NM_003126.4:c.1698C>T MANE Select | NP_003117.2:p.Ala566= |