HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55154796T>C , CM000681.2:g.55154796T>C | GRCh38 |
NC_000019.9:g.55666164T>C , CM000681.1:g.55666164T>C | GRCh37 |
NC_000019.8:g.60357976T>C | NCBI36 |
NG_007866.2:g.7937A>G , LRG_432:g.7937A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.317A>G MANE Select | ENSP00000341838.5:p.Lys106Arg | |
ENST00000665070.1:c.317A>G | ENSP00000499482.1:p.Lys106Arg | |
ENST00000344887.9:c.317A>G | ENSP00000341838.5:p.Lys106Arg | |
ENST00000585806.5:n.316A>G | ||
ENST00000586669.5:n.325A>G | ||
ENST00000587176.5:n.501A>G | ||
ENST00000587871.1:c.936A>G | ||
ENST00000588882.1:c.242A>G | ENSP00000466729.1:p.Lys81Arg | |
ENST00000590463.1:n.489A>G | ||
NM_000363.4:c.317A>G , LRG_432t1:c.317A>G | NP_000354.4:p.Lys106Arg | |
NM_000363.5:c.317A>G MANE Select | NP_000354.4:p.Lys106Arg |