Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.35576136A= , CM000679.2:g.35576136A= | GRCh38 |
| NC_000017.10:g.33903155A= , CM000679.1:g.33903155A= | GRCh37 |
| NC_000017.9:g.30927268A= | NCBI36 |
| NG_008447.1:g.7502T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225873.9:c.726T= MANE Select | ENSP00000225873.3:p.Gly242= | |
| ENST00000586663.2:c.726T= | ENSP00000466894.2:p.Gly242= | |
| ENST00000225873.8:c.726T= | ENSP00000225873.3:p.Gly242= | |
| ENST00000586663.1:c.726T= | ENSP00000466894.1:p.Gly242= | |
| ENST00000613219.4:c.726T= | ENSP00000482609.1:p.Gly242= | |
| NM_000286.2:c.726T= | NP_000277.1:p.Gly242= | |
| NM_000286.3:c.726T= MANE Select | NP_000277.1:p.Gly242= |