Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7454488C= , CM000679.2:g.7454488C= | GRCh38 |
| NC_000017.10:g.7357807C= , CM000679.1:g.7357807C= | GRCh37 |
| NC_000017.9:g.7298531C= | NCBI36 |
| NG_008026.1:g.14402C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000306071.7:c.1012C= MANE Select | ENSP00000304290.2:p.His338= | |
| ENST00000306071.6:c.1012C= | ENSP00000304290.2:p.His338= | |
| ENST00000536404.6:c.796C= | ENSP00000439209.2:p.His266= | |
| ENST00000570557.5:c.675C= | ||
| ENST00000573209.1:n.1956C= | ||
| ENST00000576360.1:c.649C= | ENSP00000459092.1:p.His217= | |
| NM_000747.2:c.1012C= | NP_000738.2:p.His338= | |
| NM_000747.3:c.1012C= MANE Select | NP_000738.2:p.His338= |