Linked Data
dbSNP Id:
rs761588340
ExAC:
12:33031926 G / A
gnomAD v2:
12-33031926-G-A
gnomAD v4:
12-32878992-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.32878992G>A , CM000674.2:g.32878992G>A | GRCh38 |
| NC_000012.11:g.33031926G>A , CM000674.1:g.33031926G>A | GRCh37 |
| NC_000012.10:g.32923193G>A | NCBI36 |
| NG_009000.1:g.22855C>T , LRG_398:g.22855C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000700559.2:c.264C>T | ENSP00000515065.2:p.Tyr88= | |
| ENST00000700563.2:c.264C>T | ENSP00000515066.2:p.Tyr88= | |
| ENST00000700563.1:c.218C>T | ||
| ENST00000700564.1:n.268C>T | ||
| ENST00000700565.1:n.117C>T | ||
| ENST00000070846.11:c.264C>T | ENSP00000070846.6:p.Tyr88= | |
| ENST00000340811.9:c.264C>T MANE Select | ENSP00000342800.5:p.Tyr88= | |
| ENST00000070846.10:c.264C>T | ENSP00000070846.6:p.Tyr88= | |
| ENST00000340811.8:c.264C>T | ENSP00000342800.4:p.Tyr88= | |
| ENST00000613243.1:c.264C>T | ENSP00000478295.1:p.Tyr88= | |
| NM_001005242.2:c.264C>T | NP_001005242.2:p.Tyr88= | |
| NM_004572.3:c.264C>T , LRG_398t1:c.264C>T | NP_004563.2:p.Tyr88= | |
| NM_001005242.3:c.264C>T MANE Select | NP_001005242.2:p.Tyr88= | |
| NM_004572.4:c.264C>T | NP_004563.2:p.Tyr88= |