Canonical Allele Identifier: CA185874189
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs201721199

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128530004_128530007del , CM000670.2:g.128530004_128530007del GRCh38
NC_000008.10:g.129542250_129542253del , CM000670.1:g.129542250_129542253del GRCh37
NC_000008.9:g.129611432_129611435del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+31073_508+31076del