HGVS | Genome Assembly |
---|---|
NC_000003.12:g.129531016G>A , CM000665.2:g.129531016G>A | GRCh38 |
NC_000003.11:g.129249859G>A , CM000665.1:g.129249859G>A | GRCh37 |
NC_000003.10:g.130732549G>A | NCBI36 |
NG_009115.1:g.7378G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000296271.4:c.502G>A MANE Select | ENSP00000296271.3:p.Ala168Thr | |
ENST00000296271.3:c.502G>A | ENSP00000296271.3:p.Ala168Thr | |
NM_000539.3:c.502G>A MANE Select | NP_000530.1:p.Ala168Thr |