HGVS | Genome Assembly |
---|---|
NC_000015.10:g.58401726G>A , CM000677.2:g.58401726G>A | GRCh38 |
NC_000015.9:g.58693925G>A , CM000677.1:g.58693925G>A | GRCh37 |
NC_000015.8:g.56481217G>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000558239.5:c.-172+18245C>T | ENSP00000453292.1:n.-172+18245C>T | |
ENST00000560863.5:n.415+18245C>T | ||
XR_429537.2:n.164+18245C>T | ||
XR_932289.1:n.165-16870C>T | ||
XR_001751556.2:n.216+18245C>T | ||
XR_001751557.2:n.216+18245C>T | ||
XR_001751558.2:n.216+18245C>T | ||
XR_001751559.2:n.216+18245C>T | ||
XR_001751560.2:n.216+18245C>T | ||
XR_001751563.2:n.216+18245C>T | ||
XR_001751565.2:n.217-13230C>T | ||
XR_429537.4:n.216+18245C>T |