Canonical Allele Identifier: CA1818922629
Gene: LINC00824 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128531740T= , CM000670.2:g.128531740T= GRCh38
NC_000008.10:g.129543986T= , CM000670.1:g.129543986T= GRCh37
NC_000008.9:g.129613168T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+29330A=