Canonical Allele Identifier: CA13409624

Gene: LINC02752

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.11206827C>G , CM000673.2:g.11206827C>G	GRCh38
NC_000011.9:g.11228374C>G , CM000673.1:g.11228374C>G	GRCh37
NC_000011.8:g.11184950C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001748132.1:n.3406-21252C>G