Canonical Allele Identifier: CA656155529
Gene: CEP152 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48700600T>G , CM000677.2:g.48700600T>G GRCh38
NC_000015.9:g.48992797T>G , CM000677.1:g.48992797T>G GRCh37
NC_000015.8:g.46780089T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_931770.1:n.5210+16418A>C
XR_931771.1:n.5210+16418A>C
XR_931772.1:n.5210+16418A>C
XR_931773.1:n.5210+16418A>C
XR_931775.1:n.5180+16418A>C
XR_001751153.2:n.5295+16418A>C
XR_931770.3:n.5196+16418A>C
XR_931775.3:n.5166+16418A>C