HGVS | Genome Assembly |
---|---|
NC_000001.11:g.1014077A>G , CM000663.2:g.1014077A>G | GRCh38 |
NC_000001.10:g.949457A>G , CM000663.1:g.949457A>G | GRCh37 |
NC_000001.9:g.939320A>G | NCBI36 |
NG_033033.1:g.5611A>G | |
NG_033033.2:g.17940A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000624697.4:c.73A>G | ENSP00000485643.1:p.Thr25Ala | |
ENST00000649529.1:c.97A>G MANE Select | ENSP00000496832.1:p.Thr33Ala | |
ENST00000379389.4:c.97A>G | ENSP00000368699.4:p.Thr33Ala | |
ENST00000624652.1:c.73A>G | ENSP00000485313.1:p.Thr25Ala | |
ENST00000624697.3:c.73A>G | ENSP00000485643.1:p.Thr25Ala | |
NM_005101.3:c.97A>G | NP_005092.1:p.Thr33Ala | |
NM_005101.4:c.97A>G MANE Select | NP_005092.1:p.Thr33Ala |