HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55157099C>T , CM000681.2:g.55157099C>T | GRCh38 |
NC_000019.9:g.55668467C>T , CM000681.1:g.55668467C>T | GRCh37 |
NC_000019.8:g.60360279C>T | NCBI36 |
NG_007866.2:g.5634G>A , LRG_432:g.5634G>A | |
NG_032759.1:g.14624G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.59G>A MANE Select | ENSP00000341838.5:p.Arg20Lys | |
ENST00000665070.1:c.59G>A | ENSP00000499482.1:p.Arg20Lys | |
ENST00000344887.9:c.59G>A | ENSP00000341838.5:p.Arg20Lys | |
ENST00000586446.1:n.201G>A | ||
ENST00000586669.5:n.67G>A | ||
ENST00000587176.5:n.243G>A | ||
ENST00000587871.1:c.678G>A | ||
ENST00000590463.1:n.231G>A | ||
NM_000363.4:c.59G>A , LRG_432t1:c.59G>A | NP_000354.4:p.Arg20Lys | |
NM_000363.5:c.59G>A MANE Select | NP_000354.4:p.Arg20Lys |