Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7454343G= , CM000679.2:g.7454343G= | GRCh38 |
| NC_000017.10:g.7357662G= , CM000679.1:g.7357662G= | GRCh37 |
| NC_000017.9:g.7298386G= | NCBI36 |
| NG_008026.1:g.14257G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000306071.7:c.867G= MANE Select | ENSP00000304290.2:p.Val289= | |
| ENST00000306071.6:c.867G= | ENSP00000304290.2:p.Val289= | |
| ENST00000536404.6:c.651G= | ENSP00000439209.2:p.Val217= | |
| ENST00000570557.5:c.530G= | ||
| ENST00000573209.1:n.1811G= | ||
| ENST00000576360.1:c.605-101G= | ENSP00000459092.1:n.605-101G= | |
| NM_000747.2:c.867G= | NP_000738.2:p.Val289= | |
| NM_000747.3:c.867G= MANE Select | NP_000738.2:p.Val289= |