Canonical Allele Identifier: CA2002992396
Gene: CEP164 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117317446C= , CM000673.2:g.117317446C= GRCh38
NC_000011.9:g.117188162C= , CM000673.1:g.117188162C= GRCh37
NC_000011.8:g.116693372C= NCBI36
NG_029372.1:g.3811G=
NG_033032.1:g.669C=

Transcript Alleles

HGVS Amino-acid change
ENST00000525734.5:c.-98+2718C= ENSP00000436609.1:n.-98+2718C=
XM_017017364.1:c.-98+913C= XP_016872853.1:n.-98+913C=