HGVS | Genome Assembly |
---|---|
NC_000011.10:g.124872931C>A , CM000673.2:g.124872931C>A | GRCh38 |
NC_000011.9:g.124742827C>A , CM000673.1:g.124742827C>A | GRCh37 |
NC_000011.8:g.124248037C>A | NCBI36 |
NG_016214.1:g.12523C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000397801.6:c.1378C>A MANE Select | ENSP00000380903.1:p.Gln460Lys | |
ENST00000397801.5:c.1378C>A | ENSP00000380903.1:p.Gln460Lys | |
ENST00000538940.5:c.1312C>A | ENSP00000441797.1:p.Gln438Lys | |
NM_022370.3:c.1378C>A | NP_071765.2:p.Gln460Lys | |
XM_011542953.1:c.2350C>A | XP_011541255.1:p.Gln784Lys | |
XM_017018122.1:c.1312C>A | XP_016873611.1:p.Gln438Lys | |
NM_022370.4:c.1378C>A MANE Select | NP_071765.2:p.Gln460Lys |