Canonical Allele Identifier: CA1818909482
Gene: LINC00824 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128547117G= , CM000670.2:g.128547117G= GRCh38
NC_000008.10:g.129559363G= , CM000670.1:g.129559363G= GRCh37
NC_000008.9:g.129628545G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+13953C=