Canonical Allele Identifier: CA672246888

Gene: CEP164

Linked Data

• dbSNP Id: rs1310878435
• MyVariant Identifiers: chr11:g.117188050G>A (hg19) ; chr11:g.117317334G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.117317334G>A , CM000673.2:g.117317334G>A	GRCh38
NC_000011.9:g.117188050G>A , CM000673.1:g.117188050G>A	GRCh37
NC_000011.8:g.116693260G>A	NCBI36
NG_029372.1:g.3923C>T
NG_033032.1:g.557G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000525734.5:c.-98+2606G>A	ENSP00000436609.1:n.-98+2606G>A
XM_017017364.1:c.-98+801G>A	XP_016872853.1:n.-98+801G>A