Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.175443899A= , CM000667.2:g.175443899A= | GRCh38 |
| NC_000005.9:g.174870902A= , CM000667.1:g.174870902A= | GRCh37 |
| NC_000005.8:g.174803508A= | NCBI36 |
| NG_011802.1:g.5262T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000794.5:c.-684T= MANE Select | NP_000785.1:n.-684T= |
| ENST00000393752.3:c.-684T= MANE Select | ENSP00000377353.1:n.-684T= |
| NM_000794.3:c.-684T= | NP_000785.1:n.-684T= |
| NM_000794.4:c.-684T= | NP_000785.1:n.-684T= |
| ENST00000393752.2:c.-684T= | ENSP00000377353.1:n.-684T= |