Canonical Allele Identifier: CA2002992409
Gene: CEP164 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117317472A= , CM000673.2:g.117317472A= GRCh38
NC_000011.9:g.117188188A= , CM000673.1:g.117188188A= GRCh37
NC_000011.8:g.116693398A= NCBI36
NG_029372.1:g.3785T=
NG_033032.1:g.695A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525734.5:c.-98+2744A= ENSP00000436609.1:n.-98+2744A=
XM_017017364.1:c.-98+939A= XP_016872853.1:n.-98+939A=
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