Canonical Allele Identifier: CA14610122

Gene: LINC01924

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.64210542C>T , CM000680.2:g.64210542C>T	GRCh38
NC_000018.9:g.61877777C>T , CM000680.1:g.61877777C>T	GRCh37
NC_000018.8:g.60028757C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_033881.1:n.201-38759C>T