Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.66560681T= , CM000673.2:g.66560681T= | GRCh38 |
| NC_000011.9:g.66328152T= , CM000673.1:g.66328152T= | GRCh37 |
| NC_000011.8:g.66084728T= | NCBI36 |
| NG_013304.2:g.18762T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000513398.2:c.1786T= MANE Select | ENSP00000426797.1:p.Tyr596= | |
| ENST00000502692.5:c.1915T= | ENSP00000422007.1:p.Tyr639= | |
| ENST00000513398.1:c.1786T= | ENSP00000426797.1:p.Tyr596= | |
| NM_001104.3:c.1786T= | NP_001095.2:p.Tyr596= | |
| NM_001258371.2:c.1915T= | NP_001245300.2:p.Tyr639= | |
| NM_001104.4:c.1786T= MANE Select | NP_001095.2:p.Tyr596= | |
| NM_001258371.3:c.1915T= | NP_001245300.2:p.Tyr639= |