HGVS | Genome Assembly |
---|---|
NC_000024.10:g.20759931A>T , CM000686.2:g.20759931A>T | GRCh38 |
NC_000024.9:g.22921817A>T , CM000686.1:g.22921817A>T | GRCh37 |
NC_000024.8:g.21331205A>T | NCBI36 |
NG_032924.1:g.8864A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000629237.2:c.145A>T MANE Select | ENSP00000486252.1:p.Arg49Trp | |
ENST00000629237.1:c.145A>T | ENSP00000486252.1:p.Arg49Trp | |
NM_001039567.2:c.145A>T | NP_001034656.1:p.Arg49Trp | |
XM_011531423.1:c.94A>T | XP_011529725.1:p.Arg32Trp | |
NM_001039567.3:c.145A>T MANE Select | NP_001034656.1:p.Arg49Trp |