Canonical Allele Identifier: CA1818922596
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816119797

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128531682_128531694del , CM000670.2:g.128531682_128531694del GRCh38
NC_000008.10:g.129543928_129543940del , CM000670.1:g.129543928_129543940del GRCh37
NC_000008.9:g.129613110_129613122del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+29377_508+29389del