Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7502634G>A , CM000679.2:g.7502634G>A | GRCh38 |
| NC_000017.10:g.7405953G>A , CM000679.1:g.7405953G>A | GRCh37 |
| NC_000017.9:g.7346677G>A | NCBI36 |
| NG_027747.1:g.23256G>A | |
| NG_027747.2:g.23256G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000937.5:c.2689G>A MANE Select | NP_000928.1:p.Ala897Thr |
| NM_000937.4:c.2689G>A | NP_000928.1:p.Ala897Thr |
| ENST00000576114.1:n.155G>A | |
| ENST00000617998.4:c.2689G>A | ENSP00000480158.1:p.Ala897Thr |
| ENST00000617998.6:n.3088G>A | |
| ENST00000621442.4:c.2689G>A | ENSP00000483957.1:p.Ala897Thr |
| ENST00000674977.2:c.2689G>A | ENSP00000502190.2:p.Ala897Thr |