HGVS | Genome Assembly |
---|---|
NC_000002.12:g.68836777G>A , CM000664.2:g.68836777G>A | GRCh38 |
NC_000002.11:g.69063909G>A , CM000664.1:g.69063909G>A | GRCh37 |
NC_000002.10:g.68917413G>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
XR_940226.1:n.431C>T (LINC01890) | ||
XR_001739529.2:n.612C>T (LINC01890) | ||
XR_001739530.1:n.862-605G>A (LINC01888) | ||
XR_940226.3:n.612C>T (LINC01890) |