Canonical Allele Identifier: CA2782164966
Gene: LINC00824 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128529859A>T , CM000670.2:g.128529859A>T GRCh38
NC_000008.10:g.129542105A>T , CM000670.1:g.129542105A>T GRCh37
NC_000008.9:g.129611287A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+31211T>A