Canonical Allele Identifier: CA10576181
Gene: CETP HGNC NCBI

Linked Data

ClinVar Variation Id: 225955
ClinVar RCV Id: RCV001682922
dbSNP Id: rs1532624

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56971567C>A , CM000678.2:g.56971567C>A GRCh38
NC_000016.9:g.57005479C>A , CM000678.1:g.57005479C>A GRCh37
NC_000016.8:g.55562980C>A NCBI36
NG_008952.1:g.14645C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000200676.8:c.658+186C>A MANE Select ENSP00000200676.3:n.658+186C>A
ENST00000200676.7:c.658+186C>A ENSP00000200676.3:n.658+186C>A
ENST00000379780.6:c.658+186C>A ENSP00000369106.2:n.658+186C>A
ENST00000566128.1:c.463+186C>A ENSP00000456276.1:n.463+186C>A
ENST00000569082.1:n.760+186C>A
NM_000078.2:c.658+186C>A NP_000069.2:n.658+186C>A
NM_001286085.1:c.658+186C>A NP_001273014.1:n.658+186C>A
XM_006721124.2:c.658+186C>A XP_006721187.1:n.658+186C>A
XM_006721124.3:c.658+186C>A XP_006721187.1:n.658+186C>A
NM_000078.3:c.658+186C>A MANE Select NP_000069.2:n.658+186C>A
NM_001286085.2:c.658+186C>A NP_001273014.1:n.658+186C>A