HGVS | Genome Assembly |
---|---|
NC_000010.11:g.92606380A>G , CM000672.2:g.92606380A>G | GRCh38 |
NC_000010.10:g.94366137A>G , CM000672.1:g.94366137A>G | GRCh37 |
NC_000010.9:g.94356117A>G | NCBI36 |
NG_032580.1:g.18313A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000260731.5:c.193A>G MANE Select | ENSP00000260731.3:p.Thr65Ala | |
ENST00000676621.1:c.193A>G | ENSP00000503639.1:p.Thr65Ala | |
ENST00000676647.1:c.-15A>G | ENSP00000503394.1:n.-15A>G | |
ENST00000676757.1:c.-15A>G | ENSP00000504289.1:n.-15A>G | |
ENST00000677720.1:c.193A>G | ENSP00000504840.1:p.Thr65Ala | |
ENST00000260731.4:c.193A>G | ENSP00000260731.3:p.Thr65Ala | |
NM_004523.3:c.193A>G | NP_004514.2:p.Thr65Ala | |
NM_004523.4:c.193A>G MANE Select | NP_004514.2:p.Thr65Ala |