Canonical Allele Identifier: CA229356658
Gene: CEP164 HGNC NCBI

Linked Data

dbSNP Id: rs376572334 rs2133528731
gnomAD v3: 11-117317388-A-G
gnomAD v4: 11-117317388-A-G
MyVariant Identifiers: chr11:g.117188104A>G (hg19) chr11:g.117317388A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117317388A>G , CM000673.2:g.117317388A>G GRCh38
NC_000011.9:g.117188104A>G , CM000673.1:g.117188104A>G GRCh37
NC_000011.8:g.116693314A>G NCBI36
NG_029372.1:g.3869T>C
NG_033032.1:g.611A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000525734.5:c.-98+2660A>G ENSP00000436609.1:n.-98+2660A>G
XM_017017364.1:c.-98+855A>G XP_016872853.1:n.-98+855A>G
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