HGVS | Genome Assembly |
---|---|
NC_000015.10:g.80152886A>T , CM000677.2:g.80152886A>T | GRCh38 |
NC_000015.9:g.80445228A>T , CM000677.1:g.80445228A>T | GRCh37 |
NC_000015.8:g.78232283A>T | NCBI36 |
NG_012833.1:g.4888A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000558767.6:c.-169A>T | ENSP00000507680.1:n.-169A>T | |
ENST00000261755.9:c.-30+45A>T | ENSP00000261755.5:n.-30+45A>T | |
ENST00000407106.5:c.-49A>T | ENSP00000385080.1:n.-49A>T | |
ENST00000537726.5:n.53+45A>T | ||
ENST00000558022.5:c.-29-140A>T | ENSP00000453152.1:n.-29-140A>T | |
ENST00000558767.5:n.93A>T | ||
ENST00000561369.1:n.32A>T | ||
XM_024449872.1:c.-49A>T | XP_024305640.1:n.-49A>T | |
NM_001374377.1:c.-49A>T | NP_001361306.1:n.-49A>T | |
NM_001374380.1:c.-30+45A>T | NP_001361309.1:n.-30+45A>T |