Canonical Allele Identifier: CA1381485596
Gene: LINC00506 HGNC NCBI

Linked Data

dbSNP Id: rs1704496932

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87124234A>T , CM000665.2:g.87124234A>T GRCh38
NC_000003.11:g.87173384A>T , CM000665.1:g.87173384A>T GRCh37
NC_000003.10:g.87256074A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104153.1:n.329-30104A>T