Canonical Allele Identifier: CA847303933

Gene: LINC00824

Linked Data

• dbSNP Id: rs1343100595
• MyVariant Identifiers: chr8:g.129559176_129559177insT (hg19) ; chr8:g.128546930_128546931insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128546935dup , CM000670.2:g.128546935dup	GRCh38
NC_000008.10:g.129559181dup , CM000670.1:g.129559181dup	GRCh37
NC_000008.9:g.129628363dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121672.1:n.508+14139dup