Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8016507G>A , CM000679.2:g.8016507G>A | GRCh38 |
| NC_000017.10:g.7919825G>A , CM000679.1:g.7919825G>A | GRCh37 |
| NC_000017.9:g.7860550G>A | NCBI36 |
| NG_009092.1:g.18838G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000180.4:c.3289G>A MANE Select | NP_000171.1:p.Ala1097Thr |
| ENST00000254854.5:c.3289G>A MANE Select | ENSP00000254854.4:p.Ala1097Thr |
| NM_000180.3:c.3289G>A | NP_000171.1:p.Ala1097Thr |
| ENST00000254854.4:c.3289G>A | ENSP00000254854.4:p.Ala1097Thr |
| ENST00000574510.1:n.227G>A | |
| XM_011523816.1:c.3289G>A | XP_011522118.1:p.Ala1097Thr |