Canonical Allele Identifier: CA185876351

Gene: LINC00824

Linked Data

• dbSNP Id: rs996465094
• gnomAD v2: 8-129559187-C-T
• gnomAD v3: 8-128546941-C-T
• gnomAD v4: 8-128546941-C-T
• MyVariant Identifiers: chr8:g.129559187C>T (hg19) ; chr8:g.128546941C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128546941C>T , CM000670.2:g.128546941C>T	GRCh38
NC_000008.10:g.129559187C>T , CM000670.1:g.129559187C>T	GRCh37
NC_000008.9:g.129628369C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121672.1:n.508+14129G>A