Canonical Allele Identifier: CA2725030495
Gene: CEP164 HGNC NCBI

Linked Data

dbSNP Id: rs2133528905

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117317492T>A , CM000673.2:g.117317492T>A GRCh38
NC_000011.9:g.117188208T>A , CM000673.1:g.117188208T>A GRCh37
NC_000011.8:g.116693418T>A NCBI36
NG_029372.1:g.3765A>T
NG_033032.1:g.715T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000525734.5:c.-98+2764T>A ENSP00000436609.1:n.-98+2764T>A
XM_017017364.1:c.-98+959T>A XP_016872853.1:n.-98+959T>A