Canonical Allele Identifier: CA15842826

Gene: LINC02883

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.85756967G>A , CM000677.2:g.85756967G>A	GRCh38
NC_000015.9:g.86300198G>A , CM000677.1:g.86300198G>A	GRCh37
NC_000015.8:g.84101202G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120366.1:n.419+917C>T