Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.64758698A= , CM000673.2:g.64758698A= | GRCh38 |
| NC_000011.9:g.64526170A= , CM000673.1:g.64526170A= | GRCh37 |
| NC_000011.8:g.64282746A= | NCBI36 |
| NG_013018.1:g.7018T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000164139.4:c.250T= MANE Select | ENSP00000164139.3:p.Tyr84= | |
| ENST00000164139.3:c.250T= | ENSP00000164139.3:p.Tyr84= | |
| ENST00000377432.7:c.244-432T= | ENSP00000366650.3:n.244-432T= | |
| NM_001164716.1:c.244-432T= | NP_001158188.1:n.244-432T= | |
| NM_005609.2:c.250T= | NP_005600.1:p.Tyr84= | |
| NM_005609.3:c.250T= | NP_005600.1:p.Tyr84= | |
| NM_005609.4:c.250T= MANE Select | NP_005600.1:p.Tyr84= |