Canonical Allele Identifier: CA1818922556
Gene: LINC00824 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128531603G= , CM000670.2:g.128531603G= GRCh38
NC_000008.10:g.129543849G= , CM000670.1:g.129543849G= GRCh37
NC_000008.9:g.129613031G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+29467C=