Canonical Allele Identifier: CA2002992298
Gene: CEP164 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117317217A= , CM000673.2:g.117317217A= GRCh38
NC_000011.9:g.117187933A= , CM000673.1:g.117187933A= GRCh37
NC_000011.8:g.116693143A= NCBI36
NG_029372.1:g.4040T=
NG_033032.1:g.440A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525734.5:c.-98+2489A= ENSP00000436609.1:n.-98+2489A=
XM_017017364.1:c.-98+684A= XP_016872853.1:n.-98+684A=