Canonical Allele Identifier: CA2793779372
Gene: CEP164 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117317242C>G , CM000673.2:g.117317242C>G GRCh38
NC_000011.9:g.117187958C>G , CM000673.1:g.117187958C>G GRCh37
NC_000011.8:g.116693168C>G NCBI36
NG_029372.1:g.4015G>C
NG_033032.1:g.465C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000525734.5:c.-98+2514C>G ENSP00000436609.1:n.-98+2514C>G
XM_017017364.1:c.-98+709C>G XP_016872853.1:n.-98+709C>G
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