Canonical Allele Identifier: CA1818908477
Gene: LINC00824 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128546928T= , CM000670.2:g.128546928T= GRCh38
NC_000008.10:g.129559174T= , CM000670.1:g.129559174T= GRCh37
NC_000008.9:g.129628356T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+14142A=