Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17342393A= , CM000663.2:g.17342393A= | GRCh38 |
| NC_000001.10:g.17668888A= , CM000663.1:g.17668888A= | GRCh37 |
| NC_000001.9:g.17541475A= | NCBI36 |
| NG_023261.2:g.39204A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375448.4:c.926A= MANE Select | ENSP00000364597.4:p.Tyr309= | |
| NM_012387.2:c.926A= | NP_036519.2:p.Tyr309= | |
| XM_011541150.1:c.740A= | XP_011539452.1:p.Tyr247= | |
| XM_011541151.1:c.926A= | XP_011539453.1:p.Tyr309= | |
| XM_011541152.1:c.389A= | XP_011539454.1:p.Tyr130= | |
| XM_011541153.1:c.926A= | XP_011539455.1:p.Tyr309= | |
| XM_011541154.1:c.926A= | XP_011539456.1:p.Tyr309= | |
| XM_011541155.1:c.926A= | XP_011539457.1:p.Tyr309= | |
| XM_011541156.1:c.926A= | XP_011539458.1:p.Tyr309= | |
| XM_011541157.1:c.35A= | XP_011539459.1:p.Tyr12= | |
| XM_011541154.2:c.926A= | XP_011539456.1:p.Tyr309= | |
| NM_012387.3:c.926A= MANE Select | NP_036519.2:p.Tyr309= |