Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.100362846T= , CM000672.2:g.100362846T= | GRCh38 |
| NC_000010.10:g.102122603T= , CM000672.1:g.102122603T= | GRCh37 |
| NC_000010.9:g.102112593T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005063.5:c.*1913T= MANE Select | NP_005054.3:n.*1913T= |
| ENST00000370355.3:c.*1913T= MANE Select | ENSP00000359380.2:n.*1913T= |
| NM_005063.4:c.*1913T= | NP_005054.3:n.*1913T= |
| ENST00000370355.2:c.*1913T= | ENSP00000359380.2:n.*1913T= |