Canonical Allele Identifier: CA185874151

Gene: LINC00824

Linked Data

• dbSNP Id: rs999473138
• gnomAD v3: 8-128529709-T-C
• gnomAD v4: 8-128529709-T-C
• MyVariant Identifiers: chr8:g.129541955T>C (hg19) ; chr8:g.128529709T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128529709T>C , CM000670.2:g.128529709T>C	GRCh38
NC_000008.10:g.129541955T>C , CM000670.1:g.129541955T>C	GRCh37
NC_000008.9:g.129611137T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121672.1:n.508+31361A>G