Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.103458495A= , CM000672.2:g.103458495A= | GRCh38 |
| NC_000010.10:g.105218252A= , CM000672.1:g.105218252A= | GRCh37 |
| NC_000010.9:g.105208242A= | NCBI36 |
| NG_016855.1:g.5397T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001001412.4:c.257T= MANE Select | NP_001001412.3:p.Leu86= |
| ENST00000329905.6:c.257T= MANE Select | ENSP00000329926.6:p.Leu86= |
| NM_001001412.3:c.257T= | NP_001001412.3:p.Leu86= |
| ENST00000329905.5:c.257T= | ENSP00000329926.5:p.Leu86= |