Canonical Allele Identifier: CA13787089

Gene: LINC02341

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.42458457C>T , CM000675.2:g.42458457C>T	GRCh38
NC_000013.10:g.43032593C>T , CM000675.1:g.43032593C>T	GRCh37
NC_000013.9:g.41930593C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_941906.1:n.244+20985C>T
NR_135319.1:n.336+20985C>T