HGVS | Genome Assembly |
---|---|
NC_000010.11:g.62820815C>T , CM000672.2:g.62820815C>T | GRCh38 |
NC_000010.10:g.64580575C>T , CM000672.1:g.64580575C>T | GRCh37 |
NC_000010.9:g.64250581C>T | NCBI36 |
NG_008936.2:g.104086G>A , LRG_239:g.104086G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000493899.2:n.542-4846G>A | ||
XM_011539428.1:c.-90-4846G>A | XP_011537730.1:n.-90-4846G>A |