HGVS | Genome Assembly |
---|---|
NC_000015.10:g.80152853G>A , CM000677.2:g.80152853G>A | GRCh38 |
NC_000015.9:g.80445195G>A , CM000677.1:g.80445195G>A | GRCh37 |
NC_000015.8:g.78232250G>A | NCBI36 |
NG_012833.1:g.4855G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000558767.6:c.-202G>A | ENSP00000507680.1:n.-202G>A | |
ENST00000261755.9:c.-30+12G>A | ENSP00000261755.5:n.-30+12G>A | |
ENST00000407106.5:c.-82G>A | ENSP00000385080.1:n.-82G>A | |
ENST00000537726.5:n.53+12G>A | ||
ENST00000558022.5:c.-29-173G>A | ENSP00000453152.1:n.-29-173G>A | |
ENST00000558767.5:n.60G>A | ||
XM_024449872.1:c.-82G>A | XP_024305640.1:n.-82G>A | |
NM_001374377.1:c.-82G>A | NP_001361306.1:n.-82G>A | |
NM_001374380.1:c.-30+12G>A | NP_001361309.1:n.-30+12G>A |