Canonical Allele Identifier: CA585119905

Gene: LINC00824

Linked Data

• dbSNP Id: rs1192037718
• gnomAD v2: 8-129542098-T-C
• gnomAD v3: 8-128529852-T-C
• gnomAD v4: 8-128529852-T-C
• MyVariant Identifiers: chr8:g.129542098T>C (hg19) ; chr8:g.128529852T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128529852T>C , CM000670.2:g.128529852T>C	GRCh38
NC_000008.10:g.129542098T>C , CM000670.1:g.129542098T>C	GRCh37
NC_000008.9:g.129611280T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121672.1:n.508+31218A>G