Canonical Allele Identifier: CA667355776

Gene: LINC02656

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.6351298C>T , CM000672.2:g.6351298C>T	GRCh38
NC_000010.10:g.6393260C>T , CM000672.1:g.6393260C>T	GRCh37
NC_000010.9:g.6433266C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_242715.2:n.3074C>T
NR_148966.1:n.983C>T