Canonical Allele Identifier: CA1818921132
Gene: LINC00824 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128529773G= , CM000670.2:g.128529773G= GRCh38
NC_000008.10:g.129542019G= , CM000670.1:g.129542019G= GRCh37
NC_000008.9:g.129611201G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+31297C=