Canonical Allele Identifier: CA2002992308
Gene: CEP164 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117317239C= , CM000673.2:g.117317239C= GRCh38
NC_000011.9:g.117187955C= , CM000673.1:g.117187955C= GRCh37
NC_000011.8:g.116693165C= NCBI36
NG_029372.1:g.4018G=
NG_033032.1:g.462C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525734.5:c.-98+2511C= ENSP00000436609.1:n.-98+2511C=
XM_017017364.1:c.-98+706C= XP_016872853.1:n.-98+706C=