Canonical Allele Identifier: CA2002992280
Gene: CEP164 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117317163A= , CM000673.2:g.117317163A= GRCh38
NC_000011.9:g.117187879A= , CM000673.1:g.117187879A= GRCh37
NC_000011.8:g.116693089A= NCBI36
NG_029372.1:g.4094T=
NG_033032.1:g.386A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525734.5:c.-98+2435A= ENSP00000436609.1:n.-98+2435A=
XM_017017364.1:c.-98+630A= XP_016872853.1:n.-98+630A=