Canonical Allele Identifier: CA652955683

Gene: LINC00824

Linked Data

• dbSNP Id: rs1404564091
• gnomAD v3: 8-128546851-A-T
• gnomAD v4: 8-128546851-A-T
• COSMIC: COSN20756951
• MyVariant Identifiers: chr8:g.129559097A>T (hg19) ; chr8:g.128546851A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128546851A>T , CM000670.2:g.128546851A>T	GRCh38
NC_000008.10:g.129559097A>T , CM000670.1:g.129559097A>T	GRCh37
NC_000008.9:g.129628279A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121672.1:n.508+14219T>A