Canonical Allele Identifier: CA2782165608
Gene: LINC00824 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128546788G>A , CM000670.2:g.128546788G>A GRCh38
NC_000008.10:g.129559034G>A , CM000670.1:g.129559034G>A GRCh37
NC_000008.9:g.129628216G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+14282C>T