Canonical Allele Identifier: CA2517756519
Gene: CEP164 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117317386C>G , CM000673.2:g.117317386C>G GRCh38
NC_000011.9:g.117188102C>G , CM000673.1:g.117188102C>G GRCh37
NC_000011.8:g.116693312C>G NCBI36
NG_029372.1:g.3871G>C
NG_033032.1:g.609C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000525734.5:c.-98+2658C>G ENSP00000436609.1:n.-98+2658C>G
XM_017017364.1:c.-98+853C>G XP_016872853.1:n.-98+853C>G
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