Canonical Allele Identifier: CA13303261

Gene: LINC02676

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8912261A>G , CM000672.2:g.8912261A>G	GRCh38
NC_000010.10:g.8954224A>G , CM000672.1:g.8954224A>G	GRCh37
NC_000010.9:g.8994230A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_131944.1:n.176-1561A>G
XR_930641.1:n.32+153102T>C