Canonical Allele Identifier: CA911624707

Gene: LINC00506

Linked Data

• dbSNP Id: rs1234747318
• MyVariant Identifiers: chr3:g.87173223T>G (hg19) ; chr3:g.87124073T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87124073T>G , CM000665.2:g.87124073T>G	GRCh38
NC_000003.11:g.87173223T>G , CM000665.1:g.87173223T>G	GRCh37
NC_000003.10:g.87255913T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_104153.1:n.329-30265T>G