Canonical Allele Identifier: CA79020304

Gene: LINC00506

Linked Data

• dbSNP Id: rs915169691
• gnomAD v2: 3-87173234-C-T
• gnomAD v3: 3-87124084-C-T
• gnomAD v4: 3-87124084-C-T
• MyVariant Identifiers: chr3:g.87173234C>T (hg19) ; chr3:g.87124084C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87124084C>T , CM000665.2:g.87124084C>T	GRCh38
NC_000003.11:g.87173234C>T , CM000665.1:g.87173234C>T	GRCh37
NC_000003.10:g.87255924C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_104153.1:n.329-30254C>T