Canonical Allele Identifier: CA2793779373
Gene: CEP164 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117317281T>C , CM000673.2:g.117317281T>C GRCh38
NC_000011.9:g.117187997T>C , CM000673.1:g.117187997T>C GRCh37
NC_000011.8:g.116693207T>C NCBI36
NG_029372.1:g.3976A>G
NG_033032.1:g.504T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000525734.5:c.-98+2553T>C ENSP00000436609.1:n.-98+2553T>C
XM_017017364.1:c.-98+748T>C XP_016872853.1:n.-98+748T>C