Canonical Allele Identifier: CA544782023

Gene: LINC00506

Linked Data

• dbSNP Id: rs1298191341
• gnomAD v2: 3-87173267-G-A
• MyVariant Identifiers: chr3:g.87173267G>A (hg19) ; chr3:g.87124117G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87124117G>A , CM000665.2:g.87124117G>A	GRCh38
NC_000003.11:g.87173267G>A , CM000665.1:g.87173267G>A	GRCh37
NC_000003.10:g.87255957G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_104153.1:n.329-30221G>A