Canonical Allele Identifier: CA79020315
Gene: LINC00506 HGNC NCBI

Linked Data

dbSNP Id: rs1004471851
gnomAD v3: 3-87124139-C-A
gnomAD v4: 3-87124139-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87124139C>A , CM000665.2:g.87124139C>A GRCh38
NC_000003.11:g.87173289C>A , CM000665.1:g.87173289C>A GRCh37
NC_000003.10:g.87255979C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104153.1:n.329-30199C>A