Canonical Allele Identifier: CA942665853
Gene: CEP164 HGNC NCBI

Linked Data

dbSNP Id: rs2035155980
gnomAD v3: 11-117317495-A-T
gnomAD v4: 11-117317495-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117317495A>T , CM000673.2:g.117317495A>T GRCh38
NC_000011.9:g.117188211A>T , CM000673.1:g.117188211A>T GRCh37
NC_000011.8:g.116693421A>T NCBI36
NG_029372.1:g.3762T>A
NG_033032.1:g.718A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000525734.5:c.-98+2767A>T ENSP00000436609.1:n.-98+2767A>T
XM_017017364.1:c.-98+962A>T XP_016872853.1:n.-98+962A>T
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