Canonical Allele Identifier: CA2002992374
Gene: CEP164 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117317400A= , CM000673.2:g.117317400A= GRCh38
NC_000011.9:g.117188116A= , CM000673.1:g.117188116A= GRCh37
NC_000011.8:g.116693326A= NCBI36
NG_029372.1:g.3857T=
NG_033032.1:g.623A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525734.5:c.-98+2672A= ENSP00000436609.1:n.-98+2672A=
XM_017017364.1:c.-98+867A= XP_016872853.1:n.-98+867A=