Canonical Allele Identifier: CA2002992296
Gene: CEP164 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117317214G= , CM000673.2:g.117317214G= GRCh38
NC_000011.9:g.117187930G= , CM000673.1:g.117187930G= GRCh37
NC_000011.8:g.116693140G= NCBI36
NG_029372.1:g.4043C=
NG_033032.1:g.437G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525734.5:c.-98+2486G= ENSP00000436609.1:n.-98+2486G=
XM_017017364.1:c.-98+681G= XP_016872853.1:n.-98+681G=