Canonical Allele Identifier: CA1818922619
Gene: LINC00824 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128531719C= , CM000670.2:g.128531719C= GRCh38
NC_000008.10:g.129543965C= , CM000670.1:g.129543965C= GRCh37
NC_000008.9:g.129613147C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+29351G=