Canonical Allele Identifier: CA1381485388
Gene: LINC00506 HGNC NCBI

Linked Data

dbSNP Id: rs1704496013

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87124172G>A , CM000665.2:g.87124172G>A GRCh38
NC_000003.11:g.87173322G>A , CM000665.1:g.87173322G>A GRCh37
NC_000003.10:g.87256012G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104153.1:n.329-30166G>A