Canonical Allele Identifier: CA1818908479
Gene: LINC00824 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128546930A= , CM000670.2:g.128546930A= GRCh38
NC_000008.10:g.129559176A= , CM000670.1:g.129559176A= GRCh37
NC_000008.9:g.129628358A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+14140T=