Canonical Allele Identifier: CA185874157

Gene: LINC00824

Linked Data

• dbSNP Id: rs538024713
• gnomAD v2: 8-129542027-T-C
• gnomAD v3: 8-128529781-T-C
• gnomAD v4: 8-128529781-T-C
• MyVariant Identifiers: chr8:g.129542027T>C (hg19) ; chr8:g.128529781T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128529781T>C , CM000670.2:g.128529781T>C	GRCh38
NC_000008.10:g.129542027T>C , CM000670.1:g.129542027T>C	GRCh37
NC_000008.9:g.129611209T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_121672.1:n.508+31289A>G