Canonical Allele Identifier: CA2224392314
Gene: CETP HGNC NCBI

Linked Data

dbSNP Id: rs2056025310
gnomAD v4: 16-56961939-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56961939C>A , CM000678.2:g.56961939C>A GRCh38
NC_000016.9:g.56995851C>A , CM000678.1:g.56995851C>A GRCh37
NC_000016.8:g.55553352C>A NCBI36
NG_008952.1:g.5017C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000200676.7:c.-41C>A ENSP00000200676.3:n.-41C>A
ENST00000379780.6:c.-41C>A ENSP00000369106.2:n.-41C>A
NM_000078.2:c.-41C>A NP_000069.2:n.-41C>A
NM_001286085.1:c.-41C>A NP_001273014.1:n.-41C>A
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