Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.73442366T>G , CM000666.2:g.73442366T>G | GRCh38 |
| NC_000004.11:g.74308083T>G , CM000666.1:g.74308083T>G | GRCh37 |
| NC_000004.10:g.74526947T>G | NCBI36 |
| NG_023028.1:g.11151T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395792.7:c.553T>G MANE Select | ENSP00000379138.2:p.Tyr185Asp | |
| ENST00000226359.2:c.553T>G | ENSP00000226359.2:p.Tyr185Asp | |
| ENST00000395792.6:c.553T>G | ENSP00000379138.2:p.Tyr185Asp | |
| NM_001134.2:c.553T>G | NP_001125.1:p.Tyr185Asp | |
| XM_011531704.1:c.550T>G | XP_011530006.1:p.Tyr184Asp | |
| NM_001354717.1:c.79T>G | NP_001341646.1:p.Tyr27Asp | |
| NM_001134.3:c.553T>G MANE Select | NP_001125.1:p.Tyr185Asp | |
| NM_001354717.2:c.79T>G | NP_001341646.2:p.Tyr27Asp |