Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.2229116G>A , CM000663.2:g.2229116G>A | GRCh38 |
| NC_000001.10:g.2160555G>A , CM000663.1:g.2160555G>A | GRCh37 |
| NC_000001.9:g.2150415G>A | NCBI36 |
| NG_013084.1:g.5422G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003036.4:c.350G>A MANE Select | NP_003027.1:p.Gly117Asp |
| ENST00000378536.5:c.350G>A MANE Select | ENSP00000367797.4:p.Gly117Asp |
| NM_003036.3:c.350G>A | NP_003027.1:p.Gly117Asp |
| ENST00000378536.4:c.350G>A | ENSP00000367797.4:p.Gly117Asp |
| ENST00000704337.1:n.137+1592G>A | |
| XM_005244775.2:c.350G>A | XP_005244832.1:p.Gly117Asp |
| XM_005244775.3:c.350G>A | XP_005244832.1:p.Gly117Asp |