Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73329584A>C , CM000677.2:g.73329584A>C | GRCh38 |
| NC_000015.9:g.73621925A>C , CM000677.1:g.73621925A>C | GRCh37 |
| NC_000015.8:g.71408978A>C | NCBI36 |
| NG_009063.1:g.44681T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.1579T>G MANE Select | ENSP00000261917.3:p.Tyr527Asp | |
| ENST00000261917.3:c.1579T>G | ENSP00000261917.3:p.Tyr527Asp | |
| NM_005477.2:c.1579T>G | NP_005468.1:p.Tyr527Asp | |
| XM_011521148.1:c.361T>G | XP_011519450.1:p.Tyr121Asp | |
| XM_011521148.2:c.361T>G | XP_011519450.1:p.Tyr121Asp | |
| NM_005477.3:c.1579T>G MANE Select | NP_005468.1:p.Tyr527Asp |