HGVS | Genome Assembly |
---|---|
NC_000020.11:g.57562852A>C , CM000682.2:g.57562852A>C | GRCh38 |
NC_000020.10:g.56137908A>C , CM000682.1:g.56137908A>C | GRCh37 |
NC_000020.9:g.55571314A>C | NCBI36 |
NG_008205.1:g.6772A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000319441.6:c.563A>C MANE Select | ENSP00000319814.4:p.Glu188Ala | |
ENST00000319441.5:c.563A>C | ENSP00000319814.4:p.Glu188Ala | |
ENST00000467047.1:n.1773A>C | ||
ENST00000470051.1:n.19A>C | ||
ENST00000498194.1:n.505A>C | ||
NM_002591.3:c.563A>C | NP_002582.3:p.Glu188Ala | |
XM_011528839.1:c.167A>C | XP_011527141.1:p.Glu56Ala | |
XM_024451888.1:c.167A>C | XP_024307656.1:p.Glu56Ala | |
NM_002591.4:c.563A>C MANE Select | NP_002582.3:p.Glu188Ala |