Canonical Allele Identifier: CA79020312

Gene: LINC00506

Linked Data

• dbSNP Id: rs894838670
• MyVariant Identifiers: chr3:g.87173285T>C (hg19) ; chr3:g.87124135T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87124135T>C , CM000665.2:g.87124135T>C	GRCh38
NC_000003.11:g.87173285T>C , CM000665.1:g.87173285T>C	GRCh37
NC_000003.10:g.87255975T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_104153.1:n.329-30203T>C