Canonical Allele Identifier: CA2002992327
Gene: CEP164 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117317276C= , CM000673.2:g.117317276C= GRCh38
NC_000011.9:g.117187992C= , CM000673.1:g.117187992C= GRCh37
NC_000011.8:g.116693202C= NCBI36
NG_029372.1:g.3981G=
NG_033032.1:g.499C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525734.5:c.-98+2548C= ENSP00000436609.1:n.-98+2548C=
XM_017017364.1:c.-98+743C= XP_016872853.1:n.-98+743C=