Canonical Allele Identifier: CA1818921159
Gene: LINC00824 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128529805A= , CM000670.2:g.128529805A= GRCh38
NC_000008.10:g.129542051A= , CM000670.1:g.129542051A= GRCh37
NC_000008.9:g.129611233A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+31265T=