Canonical Allele Identifier: CA617836087
Gene: CEP152 HGNC NCBI

Linked Data

dbSNP Id: rs1433265277

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48700603C>A , CM000677.2:g.48700603C>A GRCh38
NC_000015.9:g.48992800C>A , CM000677.1:g.48992800C>A GRCh37
NC_000015.8:g.46780092C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_931770.1:n.5210+16415G>T
XR_931771.1:n.5210+16415G>T
XR_931772.1:n.5210+16415G>T
XR_931773.1:n.5210+16415G>T
XR_931775.1:n.5180+16415G>T
XR_001751153.2:n.5295+16415G>T
XR_931770.3:n.5196+16415G>T
XR_931775.3:n.5166+16415G>T