Canonical Allele Identifier: CA10654535
Gene: CETP HGNC NCBI
MyVariant.info:
GRCh38 chr16:g.56961915G>A
GRCh37 chr16:g.56995827G>A
gnomAD v2:
16:56995827 G / A
gnomAD v3:
16:56961915 G / A
gnomAD v4:
chr16-56961915-G-A
Joint Max Group AF 0.06411994 (AFR)
Genomes Max Group AF 0.06529128 (AFR)
Exomes Max Group AF 0.06049299 (AFR)
ClinVar RCV:
RCV000378884
RCV001653770
ClinVar Variation:
369115
dbSNP:
17231520
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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
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