Canonical Allele Identifier: CA1818917157
Gene: LINC00824 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128554878C= , CM000670.2:g.128554878C= GRCh38
NC_000008.10:g.129567124C= , CM000670.1:g.129567124C= GRCh37
NC_000008.9:g.129636306C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+6192G=