Canonical Allele Identifier: CA1818921136
Gene: LINC00824 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128529781T= , CM000670.2:g.128529781T= GRCh38
NC_000008.10:g.129542027T= , CM000670.1:g.129542027T= GRCh37
NC_000008.9:g.129611209T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+31289A=