Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.1236259C>A , CM000669.2:g.1236259C>A | GRCh38 |
| NC_000007.13:g.1275895C>A , CM000669.1:g.1275895C>A | GRCh37 |
| NC_000007.12:g.1242421C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001080461.3:c.878C>A MANE Select | NP_001073930.1:p.Ala293Asp |
| ENST00000316333.9:c.878C>A MANE Select | ENSP00000314480.8:p.Ala293Asp |
| NM_001080461.1:c.878C>A | NP_001073930.1:p.Ala293Asp |
| NM_001080461.2:c.878C>A | NP_001073930.1:p.Ala293Asp |
| ENST00000316333.8:c.878C>A | ENSP00000314480.8:p.Ala293Asp |