HGVS | Genome Assembly |
---|---|
NC_000006.12:g.151615665A>C , CM000668.2:g.151615665A>C | GRCh38 |
NC_000006.11:g.151936800A>C , CM000668.1:g.151936800A>C | GRCh37 |
NC_000006.10:g.151978493A>C | NCBI36 |
NG_021198.1:g.126626A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000239374.8:c.1933A>C MANE Select | ENSP00000239374.6:p.Lys645Gln | |
ENST00000239374.7:c.1933A>C | ENSP00000239374.6:p.Lys645Gln | |
NM_025059.3:c.1933A>C | NP_079335.2:p.Lys645Gln | |
XM_011536147.1:c.1951A>C | XP_011534449.1:p.Lys651Gln | |
XM_011536148.1:c.1750A>C | XP_011534450.1:p.Lys584Gln | |
XM_011536147.2:c.1951A>C | XP_011534449.1:p.Lys651Gln | |
XM_011536148.2:c.1750A>C | XP_011534450.1:p.Lys584Gln | |
XR_001743865.1:n.129+1056T>G | ||
NM_025059.4:c.1933A>C MANE Select | NP_079335.2:p.Lys645Gln |