Canonical Allele Identifier: CA2503843603
Gene: CEP164 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117317250T>C , CM000673.2:g.117317250T>C GRCh38
NC_000011.9:g.117187966T>C , CM000673.1:g.117187966T>C GRCh37
NC_000011.8:g.116693176T>C NCBI36
NG_029372.1:g.4007A>G
NG_033032.1:g.473T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000525734.5:c.-98+2522T>C ENSP00000436609.1:n.-98+2522T>C
XM_017017364.1:c.-98+717T>C XP_016872853.1:n.-98+717T>C