Canonical Allele Identifier: CA2793779380
Gene: CEP164 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117317450G>A , CM000673.2:g.117317450G>A GRCh38
NC_000011.9:g.117188166G>A , CM000673.1:g.117188166G>A GRCh37
NC_000011.8:g.116693376G>A NCBI36
NG_029372.1:g.3807C>T
NG_033032.1:g.673G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000525734.5:c.-98+2722G>A ENSP00000436609.1:n.-98+2722G>A
XM_017017364.1:c.-98+917G>A XP_016872853.1:n.-98+917G>A