Canonical Allele Identifier: CA1381473390
Gene: LINC00506 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87103019A= , CM000665.2:g.87103019A= GRCh38
NC_000003.11:g.87152169A= , CM000665.1:g.87152169A= GRCh37
NC_000003.10:g.87234859A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104153.1:n.328+13412A=