HGVS | Genome Assembly |
---|---|
NC_000010.11:g.62852354A>T , CM000672.2:g.62852354A>T | GRCh38 |
NC_000010.10:g.64612114A>T , CM000672.1:g.64612114A>T | GRCh37 |
NC_000010.9:g.64282120A>T | NCBI36 |
NG_008936.2:g.72547T>A , LRG_239:g.72547T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000493899.2:n.542-36385T>A | ||
XM_011539428.1:c.-90-36385T>A | XP_011537730.1:n.-90-36385T>A |