Canonical Allele Identifier: CA1381485300
Gene: LINC00506 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87124092C= , CM000665.2:g.87124092C= GRCh38
NC_000003.11:g.87173242C= , CM000665.1:g.87173242C= GRCh37
NC_000003.10:g.87255932C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104153.1:n.329-30246C=