Canonical Allele Identifier: CA847293995

Gene: LINC00824

Linked Data

• dbSNP Id: rs1404200606
• gnomAD v3: 8-128529872-T-G
• gnomAD v4: 8-128529872-T-G
• MyVariant Identifiers: chr8:g.129542118T>G (hg19) ; chr8:g.128529872T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128529872T>G , CM000670.2:g.128529872T>G	GRCh38
NC_000008.10:g.129542118T>G , CM000670.1:g.129542118T>G	GRCh37
NC_000008.9:g.129611300T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121672.1:n.508+31198A>C