HGVS | Genome Assembly |
---|---|
NC_000017.11:g.49991833T>A , CM000679.2:g.49991833T>A | GRCh38 |
NC_000017.10:g.48069197T>A , CM000679.1:g.48069197T>A | GRCh37 |
NC_000017.9:g.45424196T>A | NCBI36 |
NG_023063.1:g.8392A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000434704.2:c.548A>T MANE Select | ENSP00000389870.2:p.Lys183Met | |
ENST00000512495.2:c.188A>T | ENSP00000449976.1:p.Lys63Met | |
NM_005220.2:c.548A>T | NP_005211.1:p.Lys183Met | |
XM_011524458.1:c.516+1567A>T | XP_011522760.1:n.516+1567A>T | |
NM_005220.3:c.548A>T MANE Select | NP_005211.1:p.Lys183Met |