HGVS | Genome Assembly |
---|---|
NC_000001.11:g.1014293G>A , CM000663.2:g.1014293G>A | GRCh38 |
NC_000001.10:g.949673G>A , CM000663.1:g.949673G>A | GRCh37 |
NC_000001.9:g.939536G>A | NCBI36 |
NG_033033.1:g.5827G>A | |
NG_033033.2:g.18156G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000624697.4:c.289G>A | ENSP00000485643.1:p.Ala97Thr | |
ENST00000649529.1:c.313G>A MANE Select | ENSP00000496832.1:p.Ala105Thr | |
ENST00000379389.4:c.313G>A | ENSP00000368699.4:p.Ala105Thr | |
ENST00000624652.1:c.289G>A | ENSP00000485313.1:p.Ala97Thr | |
ENST00000624697.3:c.289G>A | ENSP00000485643.1:p.Ala97Thr | |
NM_005101.3:c.313G>A | NP_005092.1:p.Ala105Thr | |
NM_005101.4:c.313G>A MANE Select | NP_005092.1:p.Ala105Thr |