Canonical Allele Identifier: CA1818917151

Gene: LINC00824

Linked Data

• dbSNP Id: rs1816497506

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128554873A>T , CM000670.2:g.128554873A>T	GRCh38
NC_000008.10:g.129567119A>T , CM000670.1:g.129567119A>T	GRCh37
NC_000008.9:g.129636301A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_121672.1:n.508+6197T>A