HGVS | Genome Assembly |
---|---|
NC_000017.11:g.6780523A>G , CM000679.2:g.6780523A>G | GRCh38 |
NC_000017.10:g.6683842A>G , CM000679.1:g.6683842A>G | GRCh37 |
NC_000017.9:g.6624566A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000321535.5:c.655A>G MANE Select | ENSP00000321386.4:p.Thr219Ala | |
ENST00000321535.4:c.655A>G | ENSP00000321386.4:p.Thr219Ala | |
NM_153230.2:c.655A>G | NP_694962.1:p.Thr219Ala | |
XM_011523697.1:c.655A>G | XP_011521999.1:p.Thr219Ala | |
XR_243544.3:n.833A>G | ||
NM_153230.3:c.655A>G MANE Select | NP_694962.1:p.Thr219Ala |