Canonical Allele Identifier: CA1818908502
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816373172

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128546962T>A , CM000670.2:g.128546962T>A GRCh38
NC_000008.10:g.129559208T>A , CM000670.1:g.129559208T>A GRCh37
NC_000008.9:g.129628390T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+14108A>T