Canonical Allele Identifier: CA1818917120
Gene: LINC00824 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128554852C= , CM000670.2:g.128554852C= GRCh38
NC_000008.10:g.129567098C= , CM000670.1:g.129567098C= GRCh37
NC_000008.9:g.129636280C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+6218G=