Canonical Allele Identifier: CA1119100825
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816373228

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128546966_128546969del , CM000670.2:g.128546966_128546969del GRCh38
NC_000008.10:g.129559212_129559215del , CM000670.1:g.129559212_129559215del GRCh37
NC_000008.9:g.129628394_129628397del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+14104_508+14107del