Canonical Allele Identifier: CA1818921089
Gene: LINC00824 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128529682A= , CM000670.2:g.128529682A= GRCh38
NC_000008.10:g.129541928A= , CM000670.1:g.129541928A= GRCh37
NC_000008.9:g.129611110A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+31388T=