Canonical Allele Identifier: CA585122929
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816378094

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128547115_128547119del , CM000670.2:g.128547115_128547119del GRCh38
NC_000008.10:g.129559361_129559365del , CM000670.1:g.129559361_129559365del GRCh37
NC_000008.9:g.129628543_129628547del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+13951_508+13955del