Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7454456T= , CM000679.2:g.7454456T= | GRCh38 |
| NC_000017.10:g.7357775T= , CM000679.1:g.7357775T= | GRCh37 |
| NC_000017.9:g.7298499T= | NCBI36 |
| NG_008026.1:g.14370T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000306071.7:c.980T= MANE Select | ENSP00000304290.2:p.Val327= | |
| ENST00000306071.6:c.980T= | ENSP00000304290.2:p.Val327= | |
| ENST00000536404.6:c.764T= | ENSP00000439209.2:p.Val255= | |
| ENST00000570557.5:c.643T= | ||
| ENST00000573209.1:n.1924T= | ||
| ENST00000576360.1:c.617T= | ENSP00000459092.1:p.Val206= | |
| NM_000747.2:c.980T= | NP_000738.2:p.Val327= | |
| NM_000747.3:c.980T= MANE Select | NP_000738.2:p.Val327= |