Canonical Allele Identifier: CA2002992318
Gene: CEP164 HGNC NCBI

Linked Data

dbSNP Id: rs1814872616

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117317256C>G , CM000673.2:g.117317256C>G GRCh38
NC_000011.9:g.117187972C>G , CM000673.1:g.117187972C>G GRCh37
NC_000011.8:g.116693182C>G NCBI36
NG_029372.1:g.4001G>C
NG_033032.1:g.479C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000525734.5:c.-98+2528C>G ENSP00000436609.1:n.-98+2528C>G
XM_017017364.1:c.-98+723C>G XP_016872853.1:n.-98+723C>G