Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7455269T>G , CM000679.2:g.7455269T>G | GRCh38 |
| NC_000017.10:g.7358588T>G , CM000679.1:g.7358588T>G | GRCh37 |
| NC_000017.9:g.7299312T>G | NCBI36 |
| NG_008026.1:g.15183T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000306071.7:c.1045-15T>G MANE Select | ENSP00000304290.2:n.1045-15T>G | |
| ENST00000306071.6:c.1045-15T>G | ENSP00000304290.2:n.1045-15T>G | |
| ENST00000536404.6:c.829-15T>G | ENSP00000439209.2:n.829-15T>G | |
| ENST00000570557.5:c.708-15T>G | ||
| ENST00000573209.1:n.1989-15T>G | ||
| ENST00000576360.1:c.682-15T>G | ENSP00000459092.1:n.682-15T>G | |
| NM_000747.2:c.1045-15T>G | NP_000738.2:n.1045-15T>G | |
| NM_000747.3:c.1045-15T>G MANE Select | NP_000738.2:n.1045-15T>G |