Canonical Allele Identifier: CA426450454

Gene: LINC01890 LINC01888

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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