Canonical Allele Identifier: CA205086243

Gene: LINC02652

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.28463177T>C , CM000672.2:g.28463177T>C	GRCh38
NC_000010.10:g.28752106T>C , CM000672.1:g.28752106T>C	GRCh37
NC_000010.9:g.28792112T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_134496.1:n.94-26956A>G