Canonical Allele Identifier: CA847303897

Gene: LINC00824

Linked Data

• dbSNP Id: rs1464010967
• gnomAD v3: 8-128546875-C-A
• gnomAD v4: 8-128546875-C-A
• MyVariant Identifiers: chr8:g.129559121C>A (hg19) ; chr8:g.128546875C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128546875C>A , CM000670.2:g.128546875C>A	GRCh38
NC_000008.10:g.129559121C>A , CM000670.1:g.129559121C>A	GRCh37
NC_000008.9:g.129628303C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121672.1:n.508+14195G>T