Canonical Allele Identifier: CA79020302

Gene: LINC00506

Linked Data

• dbSNP Id: rs1054145958
• gnomAD v2: 3-87173206-C-T
• gnomAD v3: 3-87124056-C-T
• gnomAD v4: 3-87124056-C-T
• MyVariant Identifiers: chr3:g.87173206C>T (hg19) ; chr3:g.87124056C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87124056C>T , CM000665.2:g.87124056C>T	GRCh38
NC_000003.11:g.87173206C>T , CM000665.1:g.87173206C>T	GRCh37
NC_000003.10:g.87255896C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_104153.1:n.329-30282C>T