Canonical Allele Identifier: CA13142804

Gene: LINC00709

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.9286688C>T , CM000672.2:g.9286688C>T	GRCh38
NC_000010.10:g.9328651C>T , CM000672.1:g.9328651C>T	GRCh37
NC_000010.9:g.9368657C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_108039.1:n.345C>T
NR_120635.1:n.193-2299G>A