Canonical Allele Identifier: CA847295075

Gene: LINC00824

Linked Data

• dbSNP Id: rs1479502718
• gnomAD v3: 8-128531749-A-T
• gnomAD v4: 8-128531749-A-T
• MyVariant Identifiers: chr8:g.129543995A>T (hg19) ; chr8:g.128531749A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128531749A>T , CM000670.2:g.128531749A>T	GRCh38
NC_000008.10:g.129543995A>T , CM000670.1:g.129543995A>T	GRCh37
NC_000008.9:g.129613177A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_121672.1:n.508+29321T>A