Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.103458349C>A , CM000672.2:g.103458349C>A | GRCh38 |
| NC_000010.10:g.105218106C>A , CM000672.1:g.105218106C>A | GRCh37 |
| NC_000010.9:g.105208096C>A | NCBI36 |
| NG_016855.1:g.5543G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000329905.6:c.403G>T MANE Select | ENSP00000329926.6:p.Val135Leu | |
| ENST00000329905.5:c.403G>T | ENSP00000329926.5:p.Val135Leu | |
| NM_001001412.3:c.403G>T | NP_001001412.3:p.Val135Leu | |
| NM_001001412.4:c.403G>T MANE Select | NP_001001412.3:p.Val135Leu |