Canonical Allele Identifier: CA229356611
Gene: CEP164 HGNC NCBI

Linked Data

dbSNP Id: rs1047530384
gnomAD v3: 11-117317302-G-A
gnomAD v4: 11-117317302-G-A
MyVariant Identifiers: chr11:g.117188018G>A (hg19) chr11:g.117317302G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117317302G>A , CM000673.2:g.117317302G>A GRCh38
NC_000011.9:g.117188018G>A , CM000673.1:g.117188018G>A GRCh37
NC_000011.8:g.116693228G>A NCBI36
NG_029372.1:g.3955C>T
NG_033032.1:g.525G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000525734.5:c.-98+2574G>A ENSP00000436609.1:n.-98+2574G>A
XM_017017364.1:c.-98+769G>A XP_016872853.1:n.-98+769G>A
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