Canonical Allele Identifier: CA79020292

Gene: LINC00506

Linked Data

• dbSNP Id: rs560747528
• gnomAD v2: 3-87173128-A-G
• gnomAD v3: 3-87123978-A-G
• gnomAD v4: 3-87123978-A-G
• MyVariant Identifiers: chr3:g.87173128A>G (hg19) ; chr3:g.87123978A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87123978A>G , CM000665.2:g.87123978A>G	GRCh38
NC_000003.11:g.87173128A>G , CM000665.1:g.87173128A>G	GRCh37
NC_000003.10:g.87255818A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_104153.1:n.329-30360A>G