Canonical Allele Identifier: CA185876375

Gene: LINC00824

Linked Data

• dbSNP Id: rs1006141591
• gnomAD v2: 8-129559328-T-A
• gnomAD v3: 8-128547082-T-A
• gnomAD v4: 8-128547082-T-A
• COSMIC: COSN23949515
• MyVariant Identifiers: chr8:g.129559328T>A (hg19) ; chr8:g.128547082T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128547082T>A , CM000670.2:g.128547082T>A	GRCh38
NC_000008.10:g.129559328T>A , CM000670.1:g.129559328T>A	GRCh37
NC_000008.9:g.129628510T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121672.1:n.508+13988A>T