Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46011277T= , CM000682.2:g.46011277T= | GRCh38 |
| NC_000020.10:g.44639916T= , CM000682.1:g.44639916T= | GRCh37 |
| NC_000020.9:g.44073323T= | NCBI36 |
| NG_011468.1:g.7370T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372330.3:c.784T= MANE Select | ENSP00000361405.3:p.Tyr262= | |
| NM_004994.2:c.784T= | NP_004985.2:p.Tyr262= | |
| NM_004994.3:c.784T= MANE Select | NP_004985.2:p.Tyr262= |