HGVS | Genome Assembly |
---|---|
NC_000017.11:g.49991825T>C , CM000679.2:g.49991825T>C | GRCh38 |
NC_000017.10:g.48069189T>C , CM000679.1:g.48069189T>C | GRCh37 |
NC_000017.9:g.45424188T>C | NCBI36 |
NG_023063.1:g.8400A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000434704.2:c.556A>G MANE Select | ENSP00000389870.2:p.Lys186Glu | |
ENST00000512495.2:c.196A>G | ENSP00000449976.1:p.Lys66Glu | |
NM_005220.2:c.556A>G | NP_005211.1:p.Lys186Glu | |
XM_011524458.1:c.516+1575A>G | XP_011522760.1:n.516+1575A>G | |
NM_005220.3:c.556A>G MANE Select | NP_005211.1:p.Lys186Glu |