HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55154763T>C , CM000681.2:g.55154763T>C | GRCh38 |
NC_000019.9:g.55666131T>C , CM000681.1:g.55666131T>C | GRCh37 |
NC_000019.8:g.60357943T>C | NCBI36 |
NG_007866.2:g.7970A>G , LRG_432:g.7970A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.350A>G MANE Select | ENSP00000341838.5:p.Lys117Arg | |
ENST00000665070.1:c.350A>G | ENSP00000499482.1:p.Lys117Arg | |
ENST00000344887.9:c.350A>G | ENSP00000341838.5:p.Lys117Arg | |
ENST00000585806.5:n.349A>G | ||
ENST00000586669.5:n.358A>G | ||
ENST00000587176.5:n.534A>G | ||
ENST00000587871.1:c.969A>G | ||
ENST00000588882.1:c.275A>G | ENSP00000466729.1:p.Lys92Arg | |
ENST00000590463.1:n.522A>G | ||
NM_000363.4:c.350A>G , LRG_432t1:c.350A>G | NP_000354.4:p.Lys117Arg | |
NM_000363.5:c.350A>G MANE Select | NP_000354.4:p.Lys117Arg |