Canonical Allele Identifier: CA1258845607
Gene: LINC01890 HGNC NCBI
LINC01888 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.68836777G= , CM000664.2:g.68836777G= GRCh38
NC_000002.11:g.69063909G= , CM000664.1:g.69063909G= GRCh37
NC_000002.10:g.68917413G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940226.1:n.431C= (LINC01890)
XR_001739529.2:n.612C= (LINC01890)
XR_001739530.1:n.862-605G= (LINC01888)
XR_940226.3:n.612C= (LINC01890)