Linked Data
ClinVar Variation Id:
551684
ClinVar RCV Id:
RCV000666810
dbSNP Id:
rs80356784
ExAC:
11:68548173 C / T
gnomAD v2:
11-68548173-C-T
gnomAD v3:
11-68780705-C-T
gnomAD v4:
11-68780705-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.68780705C>T , CM000673.2:g.68780705C>T | GRCh38 |
| NC_000011.9:g.68548173C>T , CM000673.1:g.68548173C>T | GRCh37 |
| NC_000011.8:g.68304749C>T | NCBI36 |
| NG_011801.1:g.66227G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000265641.10:c.1393G>A MANE Select | ENSP00000265641.4:p.Gly465Arg | |
| ENST00000265641.9:c.1393G>A | ENSP00000265641.4:p.Gly465Arg | |
| ENST00000376618.6:c.1393G>A | ENSP00000365803.2:p.Gly465Arg | |
| ENST00000539743.5:c.1393G>A | ENSP00000446108.1:p.Gly465Arg | |
| ENST00000540367.5:c.1393G>A | ENSP00000439084.1:p.Gly465Arg | |
| NM_001031847.2:c.1393G>A | NP_001027017.1:p.Gly465Arg | |
| NM_001876.3:c.1393G>A | NP_001867.2:p.Gly465Arg | |
| XM_005273762.1:c.1489G>A | XP_005273819.1:p.Gly497Arg | |
| XM_005273763.1:c.1489G>A | XP_005273820.1:p.Gly497Arg | |
| XM_005273762.3:c.1489G>A | XP_005273819.1:p.Gly497Arg | |
| XM_017017220.1:c.1393G>A | XP_016872709.1:p.Gly465Arg | |
| NM_001876.4:c.1393G>A MANE Select | NP_001867.2:p.Gly465Arg | |
| NM_001031847.3:c.1393G>A | NP_001027017.1:p.Gly465Arg |