Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46011178G= , CM000682.2:g.46011178G= | GRCh38 |
| NC_000020.10:g.44639817G= , CM000682.1:g.44639817G= | GRCh37 |
| NC_000020.9:g.44073224G= | NCBI36 |
| NG_011468.1:g.7271G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372330.3:c.685G= MANE Select | ENSP00000361405.3:p.Ala229= | |
| NM_004994.2:c.685G= | NP_004985.2:p.Ala229= | |
| NM_004994.3:c.685G= MANE Select | NP_004985.2:p.Ala229= |