Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46008928T= , CM000682.2:g.46008928T= | GRCh38 |
| NC_000020.10:g.44637567T= , CM000682.1:g.44637567T= | GRCh37 |
| NC_000020.9:g.44070974T= | NCBI36 |
| NG_011468.1:g.5021T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004994.3:c.2T= MANE Select | NP_004985.2:p.Met1= |
| ENST00000372330.3:c.2T= MANE Select | ENSP00000361405.3:p.Met1= |
| NM_004994.2:c.2T= | NP_004985.2:p.Met1= |