Canonical Allele Identifier: CA1818921245
Gene: LINC00824 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128529931T= , CM000670.2:g.128529931T= GRCh38
NC_000008.10:g.129542177T= , CM000670.1:g.129542177T= GRCh37
NC_000008.9:g.129611359T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+31139A=