Canonical Allele Identifier: CA79020295
Gene: LINC00506 HGNC NCBI

Linked Data

dbSNP Id: rs35204358

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87124011dup , CM000665.2:g.87124011dup GRCh38
NC_000003.11:g.87173161dup , CM000665.1:g.87173161dup GRCh37
NC_000003.10:g.87255851dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104153.1:n.329-30327dup