Canonical Allele Identifier: CA2175613248
Gene: CEP152 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48700636G= , CM000677.2:g.48700636G= GRCh38
NC_000015.9:g.48992833G= , CM000677.1:g.48992833G= GRCh37
NC_000015.8:g.46780125G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_931770.1:n.5210+16382C=
XR_931771.1:n.5210+16382C=
XR_931772.1:n.5210+16382C=
XR_931773.1:n.5210+16382C=
XR_931775.1:n.5180+16382C=
XR_001751153.2:n.5295+16382C=
XR_931770.3:n.5196+16382C=
XR_931775.3:n.5166+16382C=