Canonical Allele Identifier: CA2002992310
Gene: CEP164 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117317242C= , CM000673.2:g.117317242C= GRCh38
NC_000011.9:g.117187958C= , CM000673.1:g.117187958C= GRCh37
NC_000011.8:g.116693168C= NCBI36
NG_029372.1:g.4015G=
NG_033032.1:g.465C=

Transcript Alleles

HGVS Amino-acid change
ENST00000525734.5:c.-98+2514C= ENSP00000436609.1:n.-98+2514C=
XM_017017364.1:c.-98+709C= XP_016872853.1:n.-98+709C=