Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8006496T>A , CM000679.2:g.8006496T>A | GRCh38 |
| NC_000017.10:g.7909814T>A , CM000679.1:g.7909814T>A | GRCh37 |
| NC_000017.9:g.7850539T>A | NCBI36 |
| NG_009092.1:g.8827T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000180.4:c.1160T>A MANE Select | NP_000171.1:p.Val387Asp |
| ENST00000254854.5:c.1160T>A MANE Select | ENSP00000254854.4:p.Val387Asp |
| NM_000180.3:c.1160T>A | NP_000171.1:p.Val387Asp |
| ENST00000254854.4:c.1160T>A | ENSP00000254854.4:p.Val387Asp |
| XM_011523816.1:c.1160T>A | XP_011522118.1:p.Val387Asp |