HGVS | Genome Assembly |
---|---|
NC_000015.10:g.80152874G= , CM000677.2:g.80152874G= | GRCh38 |
NC_000015.9:g.80445216G= , CM000677.1:g.80445216G= | GRCh37 |
NC_000015.8:g.78232271G= | NCBI36 |
NG_012833.1:g.4876G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000558767.6:c.-181G= | ENSP00000507680.1:n.-181G= | |
ENST00000261755.9:c.-30+33G= | ENSP00000261755.5:n.-30+33G= | |
ENST00000407106.5:c.-61G= | ENSP00000385080.1:n.-61G= | |
ENST00000537726.5:n.53+33G= | ||
ENST00000558022.5:c.-29-152G= | ENSP00000453152.1:n.-29-152G= | |
ENST00000558767.5:n.81G= | ||
ENST00000561369.1:n.20G= | ||
XM_024449872.1:c.-61G= | XP_024305640.1:n.-61G= | |
NM_001374377.1:c.-61G= | NP_001361306.1:n.-61G= | |
NM_001374380.1:c.-30+33G= | NP_001361309.1:n.-30+33G= |