Linked Data
gnomAD v4:
12-57766076-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57766076T>A , CM000674.2:g.57766076T>A | GRCh38 |
| NC_000012.11:g.58159859T>A , CM000674.1:g.58159859T>A | GRCh37 |
| NC_000012.10:g.56446126T>A | NCBI36 |
| NG_007076.1:g.6118A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000546609.2:n.229A>T | ||
| ENST00000713544.1:c.317A>T | ENSP00000518840.1:p.Glu106Val | |
| ENST00000713545.1:c.317A>T | ENSP00000518841.1:p.Glu106Val | |
| ENST00000228606.9:c.317A>T MANE Select | ENSP00000228606.4:p.Glu106Val | |
| ENST00000228606.8:c.317A>T | ENSP00000228606.4:p.Glu106Val | |
| ENST00000546496.1:n.145A>T | ||
| ENST00000546609.1:c.229A>T | ||
| ENST00000547344.5:n.371A>T | ||
| ENST00000552186.1:n.436A>T | ||
| NM_000785.3:c.317A>T | NP_000776.1:p.Glu106Val | |
| NM_000785.4:c.317A>T MANE Select | NP_000776.1:p.Glu106Val |