Canonical Allele Identifier: CA1381485252
Gene: LINC00506 HGNC NCBI

Linked Data

dbSNP Id: rs1195079945

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NR_104153.1:n.329-30327G>T