Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.169510873G>A , CM000664.2:g.169510873G>A | GRCh38 |
| NC_000002.11:g.170367383G>A , CM000664.1:g.170367383G>A | GRCh37 |
| NC_000002.10:g.170075629G>A | NCBI36 |
| NG_042051.1:g.6172G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006063.3:c.1095G>A MANE Select | NP_006054.2:p.Gln365= |
| ENST00000284669.2:c.1095G>A MANE Select | ENSP00000284669.1:p.Gln365= |
| NM_006063.2:c.1095G>A | NP_006054.2:p.Gln365= |
| ENST00000284669.1:c.1095G>A | ENSP00000284669.1:p.Gln365= |
| ENST00000513963.1:c.925-3701G>A | ENSP00000424363.1:n.925-3701G>A |