Canonical Allele Identifier: CA585122917

Gene: LINC00824

Linked Data

• dbSNP Id: rs1445764740
• gnomAD v2: 8-129559229-G-A
• gnomAD v3: 8-128546983-G-A
• gnomAD v4: 8-128546983-G-A
• MyVariant Identifiers: chr8:g.129559229G>A (hg19) ; chr8:g.128546983G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128546983G>A , CM000670.2:g.128546983G>A	GRCh38
NC_000008.10:g.129559229G>A , CM000670.1:g.129559229G>A	GRCh37
NC_000008.9:g.129628411G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121672.1:n.508+14087C>T