HGVS | Genome Assembly |
---|---|
NC_000010.11:g.62850958T>A , CM000672.2:g.62850958T>A | GRCh38 |
NC_000010.10:g.64610718T>A , CM000672.1:g.64610718T>A | GRCh37 |
NC_000010.9:g.64280724T>A | NCBI36 |
NG_008936.2:g.73943A>T , LRG_239:g.73943A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000493899.2:n.542-34989A>T | ||
XM_011539428.1:c.-90-34989A>T | XP_011537730.1:n.-90-34989A>T |