Canonical Allele Identifier: CA1119097892
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816121069

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128531733G>T , CM000670.2:g.128531733G>T GRCh38
NC_000008.10:g.129543979G>T , CM000670.1:g.129543979G>T GRCh37
NC_000008.9:g.129613161G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+29337C>A