HGVS | Genome Assembly |
---|---|
NC_000001.11:g.204190713C>T , CM000663.2:g.204190713C>T | GRCh38 |
NC_000001.10:g.204159841C>T , CM000663.1:g.204159841C>T | GRCh37 |
NC_000001.9:g.202426464C>T | NCBI36 |
NG_032151.1:g.10779G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367194.5:c.188G>A MANE Select | ENSP00000356162.4:p.Arg63Lys | |
ENST00000367194.4:c.188G>A | ENSP00000356162.4:p.Arg63Lys | |
ENST00000625357.1:c.188G>A | ENSP00000485957.1:p.Arg63Lys | |
NM_002256.3:c.188G>A | NP_002247.3:p.Arg63Lys | |
XM_011509525.1:c.188G>A | XP_011507827.1:p.Arg63Lys | |
NM_002256.4:c.188G>A MANE Select | NP_002247.3:p.Arg63Lys |