Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46011158T= , CM000682.2:g.46011158T= | GRCh38 |
| NC_000020.10:g.44639797T= , CM000682.1:g.44639797T= | GRCh37 |
| NC_000020.9:g.44073204T= | NCBI36 |
| NG_011468.1:g.7251T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372330.3:c.665T= MANE Select | ENSP00000361405.3:p.Phe222= | |
| NM_004994.2:c.665T= | NP_004985.2:p.Phe222= | |
| NM_004994.3:c.665T= MANE Select | NP_004985.2:p.Phe222= |