Canonical Allele Identifier: CA2224402606
Gene: CETP HGNC NCBI

Linked Data

dbSNP Id: rs2056203257
gnomAD v4: 16-56983485-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56983485G>A , CM000678.2:g.56983485G>A GRCh38
NC_000016.9:g.57017397G>A , CM000678.1:g.57017397G>A GRCh37
NC_000016.8:g.55574898G>A NCBI36
NG_008952.1:g.26563G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000200676.8:c.1407+74G>A MANE Select ENSP00000200676.3:n.1407+74G>A
ENST00000200676.7:c.1407+74G>A ENSP00000200676.3:n.1407+74G>A
ENST00000379780.6:c.1227+74G>A ENSP00000369106.2:n.1227+74G>A
ENST00000566128.1:c.1212+74G>A ENSP00000456276.1:n.1212+74G>A
NM_000078.2:c.1407+74G>A NP_000069.2:n.1407+74G>A
NM_001286085.1:c.1227+74G>A NP_001273014.1:n.1227+74G>A
NM_000078.3:c.1407+74G>A MANE Select NP_000069.2:n.1407+74G>A
NM_001286085.2:c.1227+74G>A NP_001273014.1:n.1227+74G>A
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