Canonical Allele Identifier: CA14549559

Gene: LINC01630

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51492510C>T , CM000680.2:g.51492510C>T	GRCh38
NC_000018.9:g.49018880C>T , CM000680.1:g.49018880C>T	GRCh37
NC_000018.8:g.47272878C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040074.1:n.217-68083C>T