Canonical Allele Identifier: CA2175613263
Gene: CEP152 HGNC NCBI

Linked Data

dbSNP Id: rs1891533161

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48700697_48700702del , CM000677.2:g.48700697_48700702del GRCh38
NC_000015.9:g.48992894_48992899del , CM000677.1:g.48992894_48992899del GRCh37
NC_000015.8:g.46780186_46780191del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_931770.1:n.5210+16324_5210+16329del
XR_931771.1:n.5210+16324_5210+16329del
XR_931772.1:n.5210+16324_5210+16329del
XR_931773.1:n.5210+16324_5210+16329del
XR_931775.1:n.5180+16324_5180+16329del
XR_001751153.2:n.5295+16324_5295+16329del
XR_931770.3:n.5196+16324_5196+16329del
XR_931775.3:n.5166+16324_5166+16329del