Canonical Allele Identifier: CA11272006

Gene: LINC02583

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.46463303G>A , CM000664.2:g.46463303G>A	GRCh38
NC_000002.11:g.46690442G>A , CM000664.1:g.46690442G>A	GRCh37
NC_000002.10:g.46543946G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432241.5:n.365-20941G>A