Canonical Allele Identifier: CA2793779374
Gene: CEP164 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117317298A>C , CM000673.2:g.117317298A>C GRCh38
NC_000011.9:g.117188014A>C , CM000673.1:g.117188014A>C GRCh37
NC_000011.8:g.116693224A>C NCBI36
NG_029372.1:g.3959T>G
NG_033032.1:g.521A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000525734.5:c.-98+2570A>C ENSP00000436609.1:n.-98+2570A>C
XM_017017364.1:c.-98+765A>C XP_016872853.1:n.-98+765A>C