Linked Data
gnomAD v4:
12-57766149-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57766149T>A , CM000674.2:g.57766149T>A | GRCh38 |
| NC_000012.11:g.58159932T>A , CM000674.1:g.58159932T>A | GRCh37 |
| NC_000012.10:g.56446199T>A | NCBI36 |
| NG_007076.1:g.6045A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000546609.2:n.156A>T | ||
| ENST00000713544.1:c.244A>T | ENSP00000518840.1:p.Thr82Ser | |
| ENST00000713545.1:c.244A>T | ENSP00000518841.1:p.Thr82Ser | |
| ENST00000228606.9:c.244A>T MANE Select | ENSP00000228606.4:p.Thr82Ser | |
| ENST00000228606.8:c.244A>T | ENSP00000228606.4:p.Thr82Ser | |
| ENST00000546496.1:n.72A>T | ||
| ENST00000546609.1:c.156A>T | ||
| ENST00000547344.5:n.298A>T | ||
| ENST00000552186.1:n.363A>T | ||
| NM_000785.3:c.244A>T | NP_000776.1:p.Thr82Ser | |
| NM_000785.4:c.244A>T MANE Select | NP_000776.1:p.Thr82Ser |