Canonical Allele Identifier: CA8070715
Gene: CETP HGNC NCBI

Linked Data

dbSNP Id: rs780994834
ExAC: 16:56995852 T / C
gnomAD v2: 16-56995852-T-C
gnomAD v4: 16-56961940-T-C
MyVariant Identifiers: chr16:g.56995852T>C (hg19) chr16:g.56961940T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56961940T>C , CM000678.2:g.56961940T>C GRCh38
NC_000016.9:g.56995852T>C , CM000678.1:g.56995852T>C GRCh37
NC_000016.8:g.55553353T>C NCBI36
NG_008952.1:g.5018T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000200676.7:c.-40T>C ENSP00000200676.3:n.-40T>C
ENST00000379780.6:c.-40T>C ENSP00000369106.2:n.-40T>C
NM_000078.2:c.-40T>C NP_000069.2:n.-40T>C
NM_001286085.1:c.-40T>C NP_001273014.1:n.-40T>C
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