Linked Data
ClinVar Variation Id:
213745
dbSNP Id:
rs139858464
ExAC:
20:45354091 A / G
gnomAD v2:
20-45354091-A-G
gnomAD v3:
20-46725452-A-G
gnomAD v4:
20-46725452-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46725452A>G , CM000682.2:g.46725452A>G | GRCh38 |
| NC_000020.10:g.45354091A>G , CM000682.1:g.45354091A>G | GRCh37 |
| NC_000020.9:g.44787498A>G | NCBI36 |
| NG_016284.1:g.20813A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000359271.4:c.416A>G MANE Select | ENSP00000352216.2:p.Tyr139Cys | |
| ENST00000359271.3:c.416A>G | ENSP00000352216.2:p.Tyr139Cys | |
| ENST00000611837.1:n.568A>G | ||
| NM_030777.3:c.416A>G | NP_110404.1:p.Tyr139Cys | |
| XM_011529060.1:c.479A>G | XP_011527362.1:p.Tyr160Cys | |
| XM_011529061.1:c.425A>G | XP_011527363.1:p.Tyr142Cys | |
| XM_011529062.1:c.479A>G | XP_011527364.1:p.Tyr160Cys | |
| XM_011529063.1:c.479A>G | XP_011527365.1:p.Tyr160Cys | |
| XM_011529064.1:c.479A>G | XP_011527366.1:p.Tyr160Cys | |
| XM_011529065.1:c.479A>G | XP_011527367.1:p.Tyr160Cys | |
| XR_936641.1:n.615A>G | ||
| XM_011529060.2:c.479A>G | XP_011527362.1:p.Tyr160Cys | |
| XM_011529061.2:c.425A>G | XP_011527363.1:p.Tyr142Cys | |
| XM_011529062.2:c.479A>G | XP_011527364.1:p.Tyr160Cys | |
| XM_011529063.2:c.479A>G | XP_011527365.1:p.Tyr160Cys | |
| XM_011529064.2:c.479A>G | XP_011527366.1:p.Tyr160Cys | |
| XM_011529065.2:c.479A>G | XP_011527367.1:p.Tyr160Cys | |
| XM_017028087.2:c.416A>G | XP_016883576.1:p.Tyr139Cys | |
| XR_936641.2:n.602A>G | ||
| NM_030777.4:c.416A>G MANE Select | NP_110404.1:p.Tyr139Cys |