HGVS | Genome Assembly |
---|---|
NC_000015.10:g.58386313C>T , CM000677.2:g.58386313C>T | GRCh38 |
NC_000015.9:g.58678512C>T , CM000677.1:g.58678512C>T | GRCh37 |
NC_000015.8:g.56465804C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000558239.5:c.-172+33658G>A | ENSP00000453292.1:n.-172+33658G>A | |
ENST00000560863.5:n.415+33658G>A | ||
XR_429537.2:n.164+33658G>A | ||
XR_932289.1:n.165-1457G>A | ||
XR_001751556.2:n.216+33658G>A | ||
XR_001751557.2:n.216+33658G>A | ||
XR_001751558.2:n.216+33658G>A | ||
XR_001751559.2:n.216+33658G>A | ||
XR_001751560.2:n.216+33658G>A | ||
XR_001751563.2:n.216+33658G>A | ||
XR_001751565.2:n.2400G>A | ||
XR_429537.4:n.216+33658G>A |