Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57764172A>C , CM000674.2:g.57764172A>C | GRCh38 |
| NC_000012.11:g.58157955A>C , CM000674.1:g.58157955A>C | GRCh37 |
| NC_000012.10:g.56444222A>C | NCBI36 |
| NG_007076.1:g.8022T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000713544.1:c.1222T>G | ENSP00000518840.1:p.Tyr408Asp | |
| ENST00000713545.1:c.*146T>G | ENSP00000518841.1:n.*146T>G | |
| ENST00000228606.9:c.1141T>G MANE Select | ENSP00000228606.4:p.Tyr381Asp | |
| ENST00000228606.8:c.1141T>G | ENSP00000228606.4:p.Tyr381Asp | |
| ENST00000546567.5:c.436T>G | ENSP00000449472.1:p.Tyr146Asp | |
| ENST00000547344.5:n.1280T>G | ||
| NM_000785.3:c.1141T>G | NP_000776.1:p.Tyr381Asp | |
| NM_000785.4:c.1141T>G MANE Select | NP_000776.1:p.Tyr381Asp |