Canonical Allele Identifier: CA1381485200
Gene: LINC00506 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87123936T= , CM000665.2:g.87123936T= GRCh38
NC_000003.11:g.87173086T= , CM000665.1:g.87173086T= GRCh37
NC_000003.10:g.87255776T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104153.1:n.329-30402T=