Canonical Allele Identifier: CA2506995886
Gene: LINC00824 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128530162C>A , CM000670.2:g.128530162C>A GRCh38
NC_000008.10:g.129542408C>A , CM000670.1:g.129542408C>A GRCh37
NC_000008.9:g.129611590C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+30908G>T