Canonical Allele Identifier: CA2002992423
Gene: CEP164 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117317494T= , CM000673.2:g.117317494T= GRCh38
NC_000011.9:g.117188210T= , CM000673.1:g.117188210T= GRCh37
NC_000011.8:g.116693420T= NCBI36
NG_029372.1:g.3763A=
NG_033032.1:g.717T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525734.5:c.-98+2766T= ENSP00000436609.1:n.-98+2766T=
XM_017017364.1:c.-98+961T= XP_016872853.1:n.-98+961T=