Canonical Allele Identifier: CA911624663

Gene: LINC00506

Linked Data

• dbSNP Id: rs1456945026
• gnomAD v3: 3-87123992-C-A
• gnomAD v4: 3-87123992-C-A
• MyVariant Identifiers: chr3:g.87173142C>A (hg19) ; chr3:g.87123992C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87123992C>A , CM000665.2:g.87123992C>A	GRCh38
NC_000003.11:g.87173142C>A , CM000665.1:g.87173142C>A	GRCh37
NC_000003.10:g.87255832C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_104153.1:n.329-30346C>A