Canonical Allele Identifier: CA10654535
Gene: CETP HGNC NCBI

Linked Data

ClinVar Variation Id: 369115
dbSNP Id: rs17231520

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56961915G>A , CM000678.2:g.56961915G>A GRCh38
NC_000016.9:g.56995827G>A , CM000678.1:g.56995827G>A GRCh37
NC_000016.8:g.55553328G>A NCBI36
NG_008952.1:g.4993G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000200676.7:c.-65G>A ENSP00000200676.3:n.-65G>A