HGVS | Genome Assembly |
---|---|
NC_000015.10:g.52987181A>T , CM000677.2:g.52987181A>T | GRCh38 |
NC_000015.9:g.53279378A>T , CM000677.1:g.53279378A>T | GRCh37 |
NC_000015.8:g.51066670A>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
XR_932256.1:n.463+11332A>T | ||
XR_932257.1:n.463+11332A>T | ||
XM_017022782.1:c.*4896A>T | XP_016878271.1:n.*4896A>T | |
XM_017022783.1:c.*4896A>T | XP_016878272.1:n.*4896A>T | |
XM_017022784.1:c.451+11332A>T | XP_016878273.1:n.451+11332A>T | |
XM_017022785.1:c.451+11332A>T | XP_016878274.1:n.451+11332A>T | |
XR_001751547.1:n.5434A>T | ||
XR_001751548.1:n.552+11332A>T | ||
XR_932257.2:n.533+11332A>T | ||
XR_004837528.1:n.5584A>T | ||
XR_004837529.1:n.5519A>T | ||
XR_004837530.1:n.533+11332A>T | ||
XR_004837531.1:n.533+11332A>T |