Canonical Allele Identifier: CA2002992319
Gene: CEP164 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117317259T= , CM000673.2:g.117317259T= GRCh38
NC_000011.9:g.117187975T= , CM000673.1:g.117187975T= GRCh37
NC_000011.8:g.116693185T= NCBI36
NG_029372.1:g.3998A=
NG_033032.1:g.482T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525734.5:c.-98+2531T= ENSP00000436609.1:n.-98+2531T=
XM_017017364.1:c.-98+726T= XP_016872853.1:n.-98+726T=