Canonical Allele Identifier: CA15575722

Gene: LINC00824

Linked Data

• dbSNP Id: rs1400482
• gnomAD v2: 8-129541931-G-A
• gnomAD v3: 8-128529685-G-A
• gnomAD v4: 8-128529685-G-A
• MyVariant Identifiers: chr8:g.129541931G>A (hg19) ; chr8:g.128529685G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128529685G>A , CM000670.2:g.128529685G>A	GRCh38
NC_000008.10:g.129541931G>A , CM000670.1:g.129541931G>A	GRCh37
NC_000008.9:g.129611113G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_121672.1:n.508+31385C>T