Canonical Allele Identifier: CA585119924

Gene: LINC00824

Linked Data

• dbSNP Id: rs1165458615
• gnomAD v2: 8-129542331-C-G
• gnomAD v3: 8-128530085-C-G
• gnomAD v4: 8-128530085-C-G
• MyVariant Identifiers: chr8:g.129542331C>G (hg19) ; chr8:g.128530085C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128530085C>G , CM000670.2:g.128530085C>G	GRCh38
NC_000008.10:g.129542331C>G , CM000670.1:g.129542331C>G	GRCh37
NC_000008.9:g.129611513C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121672.1:n.508+30985G>C