Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7454547C= , CM000679.2:g.7454547C= | GRCh38 |
| NC_000017.10:g.7357866C= , CM000679.1:g.7357866C= | GRCh37 |
| NC_000017.9:g.7298590C= | NCBI36 |
| NG_008026.1:g.14461C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000306071.7:c.1044+27C= MANE Select | ENSP00000304290.2:n.1044+27C= | |
| ENST00000306071.6:c.1044+27C= | ENSP00000304290.2:n.1044+27C= | |
| ENST00000536404.6:c.828+27C= | ENSP00000439209.2:n.828+27C= | |
| ENST00000570557.5:c.707+27C= | ||
| ENST00000573209.1:n.1988+27C= | ||
| ENST00000576360.1:c.681+27C= | ENSP00000459092.1:n.681+27C= | |
| NM_000747.2:c.1044+27C= | NP_000738.2:n.1044+27C= | |
| NM_000747.3:c.1044+27C= MANE Select | NP_000738.2:n.1044+27C= |