Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.212883433T>G , CM000663.2:g.212883433T>G | GRCh38 |
| NC_000001.10:g.213056775T>G , CM000663.1:g.213056775T>G | GRCh37 |
| NC_000001.9:g.211123398T>G | NCBI36 |
| NG_028131.1:g.30179T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000366971.9:c.1087T>G MANE Select | ENSP00000355938.4:p.Tyr363Asp | |
| ENST00000366971.8:c.1087T>G | ENSP00000355938.4:p.Tyr363Asp | |
| ENST00000419102.1:c.483T>G | ||
| ENST00000474693.1:n.312T>G | ||
| ENST00000483790.1:n.25T>G | ||
| NM_014053.3:c.1087T>G | NP_054772.1:p.Tyr363Asp | |
| XM_011509446.1:c.1087T>G | XP_011507748.1:p.Tyr363Asp | |
| XR_247024.1:n.1261T>G | ||
| XR_426771.1:n.1388T>G | ||
| XM_011509446.3:c.1087T>G | XP_011507748.1:p.Tyr363Asp | |
| XR_247024.3:n.1261T>G | ||
| NM_014053.4:c.1087T>G MANE Select | NP_054772.1:p.Tyr363Asp |