Canonical Allele Identifier: CA10736760

Gene: LINC02884

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.112313948C>T , CM000663.2:g.112313948C>T	GRCh38
NC_000001.10:g.112856570C>T , CM000663.1:g.112856570C>T	GRCh37
NC_000001.9:g.112658093C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_947710.1:n.272+46414G>A
XR_001738189.1:n.317+46414G>A