Canonical Allele Identifier: CA1119097556
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816091564

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128530089_128530090del , CM000670.2:g.128530089_128530090del GRCh38
NC_000008.10:g.129542335_129542336del , CM000670.1:g.129542335_129542336del GRCh37
NC_000008.9:g.129611517_129611518del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+30980_508+30981del