Canonical Allele Identifier: CA585119929

Gene: LINC00824

Linked Data

• dbSNP Id: rs917433418
• gnomAD v2: 8-129542378-G-T
• gnomAD v3: 8-128530132-G-T
• gnomAD v4: 8-128530132-G-T
• MyVariant Identifiers: chr8:g.129542378G>T (hg19) ; chr8:g.128530132G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128530132G>T , CM000670.2:g.128530132G>T	GRCh38
NC_000008.10:g.129542378G>T , CM000670.1:g.129542378G>T	GRCh37
NC_000008.9:g.129611560G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121672.1:n.508+30938C>A