Canonical Allele Identifier: CA2002992281
Gene: CEP164 HGNC NCBI

Linked Data

dbSNP Id: rs2035146025
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117317166T>A , CM000673.2:g.117317166T>A GRCh38
NC_000011.9:g.117187882T>A , CM000673.1:g.117187882T>A GRCh37
NC_000011.8:g.116693092T>A NCBI36
NG_029372.1:g.4091A>T
NG_033032.1:g.389T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000525734.5:c.-98+2438T>A ENSP00000436609.1:n.-98+2438T>A
XM_017017364.1:c.-98+633T>A XP_016872853.1:n.-98+633T>A
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