Canonical Allele Identifier: CA185874152

Gene: LINC00824

Linked Data

• dbSNP Id: rs1033020226
• gnomAD v3: 8-128529717-G-A
• gnomAD v4: 8-128529717-G-A
• MyVariant Identifiers: chr8:g.129541963G>A (hg19) ; chr8:g.128529717G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128529717G>A , CM000670.2:g.128529717G>A	GRCh38
NC_000008.10:g.129541963G>A , CM000670.1:g.129541963G>A	GRCh37
NC_000008.9:g.129611145G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_121672.1:n.508+31353C>T