Canonical Allele Identifier: CA1818908491
Gene: LINC00824 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128546947C= , CM000670.2:g.128546947C= GRCh38
NC_000008.10:g.129559193C= , CM000670.1:g.129559193C= GRCh37
NC_000008.9:g.129628375C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+14123G=