Canonical Allele Identifier: CA2002992392
Gene: CEP164 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117317439C= , CM000673.2:g.117317439C= GRCh38
NC_000011.9:g.117188155C= , CM000673.1:g.117188155C= GRCh37
NC_000011.8:g.116693365C= NCBI36
NG_029372.1:g.3818G=
NG_033032.1:g.662C=

Transcript Alleles

HGVS Amino-acid change
ENST00000525734.5:c.-98+2711C= ENSP00000436609.1:n.-98+2711C=
XM_017017364.1:c.-98+906C= XP_016872853.1:n.-98+906C=