Linked Data
ClinVar Variation Id:
167468
dbSNP Id:
rs142720126
ExAC:
10:13325801 G / A
gnomAD v2:
10-13325801-G-A
gnomAD v3:
10-13283801-G-A
gnomAD v4:
10-13283801-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.13283801G>A , CM000672.2:g.13283801G>A | GRCh38 |
| NC_000010.10:g.13325801G>A , CM000672.1:g.13325801G>A | GRCh37 |
| NC_000010.9:g.13365807G>A | NCBI36 |
| NG_012862.1:g.21330C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000263038.9:c.717C>T MANE Select | ENSP00000263038.4:p.Tyr239= | |
| ENST00000263038.8:c.717C>T | ENSP00000263038.4:p.Tyr239= | |
| ENST00000396913.6:c.417C>T | ENSP00000380121.2:p.Tyr139= | |
| ENST00000396920.7:c.666C>T | ENSP00000380126.3:p.Tyr222= | |
| ENST00000453759.6:c.417C>T | ENSP00000412525.2:p.Tyr139= | |
| NM_001037537.1:c.417C>T | NP_001032626.1:p.Tyr139= | |
| NM_006214.3:c.717C>T | NP_006205.1:p.Tyr239= | |
| XM_005252469.2:c.498C>T | XP_005252526.1:p.Tyr166= | |
| NM_001323080.1:c.417C>T | NP_001310009.1:p.Tyr139= | |
| NM_001323082.1:c.723C>T | NP_001310011.1:p.Tyr241= | |
| NM_001323083.1:c.453C>T | NP_001310012.1:p.Tyr151= | |
| NM_001323084.1:c.423C>T | NP_001310013.1:p.Tyr141= | |
| NM_006214.4:c.717C>T MANE Select | NP_006205.1:p.Tyr239= | |
| NM_001037537.2:c.417C>T | NP_001032626.1:p.Tyr139= | |
| NM_001323080.2:c.417C>T | NP_001310009.1:p.Tyr139= | |
| NM_001323082.2:c.723C>T | NP_001310011.1:p.Tyr241= | |
| NM_001323083.2:c.453C>T | NP_001310012.1:p.Tyr151= | |
| NM_001323084.2:c.423C>T | NP_001310013.1:p.Tyr141= |