Canonical Allele Identifier: CA185874166

Gene: LINC00824

Linked Data

• dbSNP Id: rs983071572
• gnomAD v2: 8-129542106-C-T
• gnomAD v3: 8-128529860-C-T
• gnomAD v4: 8-128529860-C-T
• MyVariant Identifiers: chr8:g.129542106C>T (hg19) ; chr8:g.128529860C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128529860C>T , CM000670.2:g.128529860C>T	GRCh38
NC_000008.10:g.129542106C>T , CM000670.1:g.129542106C>T	GRCh37
NC_000008.9:g.129611288C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_121672.1:n.508+31210G>A