Linked Data
ClinVar Variation Id:
295892
dbSNP Id:
rs142071466
ExAC:
1:22211150 G / A
gnomAD v2:
1-22211150-G-A
gnomAD v3:
1-21884657-G-A
gnomAD v4:
1-21884657-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.21884657G>A , CM000663.2:g.21884657G>A | GRCh38 |
| NC_000001.10:g.22211150G>A , CM000663.1:g.22211150G>A | GRCh37 |
| NC_000001.9:g.22083737G>A | NCBI36 |
| NG_016740.1:g.57601C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374695.8:c.1525C>T MANE Select | ENSP00000363827.3:p.His509Tyr | |
| ENST00000374695.7:c.1525C>T | ENSP00000363827.3:p.His509Tyr | |
| NM_001291860.1:c.1528C>T | NP_001278789.1:p.His510Tyr | |
| NM_005529.6:c.1525C>T | NP_005520.4:p.His509Tyr | |
| XM_006710594.2:c.1576C>T | XP_006710657.1:p.His526Tyr | |
| XM_006710595.2:c.1528C>T | XP_006710658.1:p.His510Tyr | |
| XM_006710596.2:c.1579C>T | XP_006710659.1:p.His527Tyr | |
| XM_006710597.2:c.1525C>T | XP_006710660.1:p.His509Tyr | |
| XM_011541317.1:c.1579C>T | XP_011539619.1:p.His527Tyr | |
| XM_011541318.1:c.1579C>T | XP_011539620.1:p.His527Tyr | |
| XM_011541319.1:c.1579C>T | XP_011539621.1:p.His527Tyr | |
| XM_011541320.1:c.1579C>T | XP_011539622.1:p.His527Tyr | |
| XM_011541321.1:c.1579C>T | XP_011539623.1:p.His527Tyr | |
| XM_011541322.1:c.1579C>T | XP_011539624.1:p.His527Tyr | |
| XM_011541318.2:c.1579C>T | XP_011539620.1:p.His527Tyr | |
| XM_017001120.1:c.1720C>T | XP_016856609.1:p.His574Tyr | |
| XM_017001121.1:c.1669C>T | XP_016856610.1:p.His557Tyr | |
| XM_017001122.1:c.1666C>T | XP_016856611.1:p.His556Tyr | |
| NM_005529.7:c.1525C>T MANE Select | NP_005520.4:p.His509Tyr | |
| NM_001291860.2:c.1528C>T | NP_001278789.1:p.His510Tyr |