Canonical Allele Identifier: CA79020321

Gene: LINC00506

Linked Data

• dbSNP Id: rs966137272
• gnomAD v3: 3-87124178-T-C
• gnomAD v4: 3-87124178-T-C
• MyVariant Identifiers: chr3:g.87173328T>C (hg19) ; chr3:g.87124178T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87124178T>C , CM000665.2:g.87124178T>C	GRCh38
NC_000003.11:g.87173328T>C , CM000665.1:g.87173328T>C	GRCh37
NC_000003.10:g.87256018T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_104153.1:n.329-30160T>C