Canonical Allele Identifier: CA185876385

Gene: LINC00824

Linked Data

• dbSNP Id: rs928270585
• gnomAD v2: 8-129559387-T-A
• gnomAD v3: 8-128547141-T-A
• gnomAD v4: 8-128547141-T-A
• MyVariant Identifiers: chr8:g.129559387T>A (hg19) ; chr8:g.128547141T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128547141T>A , CM000670.2:g.128547141T>A	GRCh38
NC_000008.10:g.129559387T>A , CM000670.1:g.129559387T>A	GRCh37
NC_000008.9:g.129628569T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121672.1:n.508+13929A>T