Canonical Allele Identifier: CA185874442

Gene: LINC00824

Linked Data

• dbSNP Id: rs561632375
• gnomAD v3: 8-128531729-A-G
• gnomAD v4: 8-128531729-A-G
• MyVariant Identifiers: chr8:g.129543975A>G (hg19) ; chr8:g.128531729A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128531729A>G , CM000670.2:g.128531729A>G	GRCh38
NC_000008.10:g.129543975A>G , CM000670.1:g.129543975A>G	GRCh37
NC_000008.9:g.129613157A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_121672.1:n.508+29341T>C