Canonical Allele Identifier: CA847304052

Gene: LINC00824

Linked Data

• dbSNP Id: rs1227672122
• gnomAD v3: 8-128547094-GC-G
• gnomAD v4: 8-128547094-GC-G
• MyVariant Identifiers: chr8:g.129559341del (hg19) ; chr8:g.128547095del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128547095del , CM000670.2:g.128547095del	GRCh38
NC_000008.10:g.129559341del , CM000670.1:g.129559341del	GRCh37
NC_000008.9:g.129628523del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121672.1:n.508+13975del