Canonical Allele Identifier: CA2175613249
Gene: CEP152 HGNC NCBI

Linked Data

dbSNP Id: rs1891532471

Genomic Alleles

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

Transcript Alleles

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