Canonical Allele Identifier: CA847304223

Gene: LINC00824

Linked Data

• dbSNP Id: rs1478258408
• MyVariant Identifiers: chr8:g.129559388_129559389del (hg19) ; chr8:g.128547142_128547143del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128547143_128547144del , CM000670.2:g.128547143_128547144del	GRCh38
NC_000008.10:g.129559389_129559390del , CM000670.1:g.129559389_129559390del	GRCh37
NC_000008.9:g.129628571_129628572del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121672.1:n.508+13927_508+13928del