Canonical Allele Identifier: CA1119101176
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816378214

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128547117del , CM000670.2:g.128547117del GRCh38
NC_000008.10:g.129559363del , CM000670.1:g.129559363del GRCh37
NC_000008.9:g.129628545del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+13953del