Canonical Allele Identifier: CA2002992288
Gene: CEP164 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117317204G= , CM000673.2:g.117317204G= GRCh38
NC_000011.9:g.117187920G= , CM000673.1:g.117187920G= GRCh37
NC_000011.8:g.116693130G= NCBI36
NG_029372.1:g.4053C=
NG_033032.1:g.427G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525734.5:c.-98+2476G= ENSP00000436609.1:n.-98+2476G=
XM_017017364.1:c.-98+671G= XP_016872853.1:n.-98+671G=