HGVS | Genome Assembly |
---|---|
NC_000001.11:g.165419879T>G , CM000663.2:g.165419879T>G | GRCh38 |
NC_000001.10:g.165389116T>G , CM000663.1:g.165389116T>G | GRCh37 |
NC_000001.9:g.163655740T>G | NCBI36 |
NG_029517.1:g.30477A>C | |
NG_029517.2:g.30477A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000359842.10:c.433A>C MANE Select | ENSP00000352900.5:p.Arg145= | |
ENST00000359842.9:c.433A>C | ENSP00000352900.5:p.Arg145= | |
ENST00000470566.1:n.358A>C | ||
ENST00000619224.1:c.64A>C | ENSP00000482458.1:p.Arg22= | |
NM_001256570.1:c.64A>C | NP_001243499.1:p.Arg22= | |
NM_001256571.1:c.64A>C | NP_001243500.1:p.Arg22= | |
NM_006917.4:c.433A>C | NP_008848.1:p.Arg145= | |
NM_006917.5:c.433A>C MANE Select | NP_008848.1:p.Arg145= | |
NM_001256571.2:c.64A>C | NP_001243500.1:p.Arg22= | |
NM_001256570.2:c.64A>C | NP_001243499.1:p.Arg22= |