Canonical Allele Identifier: CA2224395669
Gene: CETP HGNC NCBI

Linked Data

dbSNP Id: rs9939224

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56968820T>A , CM000678.2:g.56968820T>A GRCh38
NC_000016.9:g.57002732T>A , CM000678.1:g.57002732T>A GRCh37
NC_000016.8:g.55560233T>A NCBI36
NG_008952.1:g.11898T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000200676.8:c.234-566T>A MANE Select ENSP00000200676.3:n.234-566T>A
ENST00000200676.7:c.234-566T>A ENSP00000200676.3:n.234-566T>A
ENST00000379780.6:c.234-566T>A ENSP00000369106.2:n.234-566T>A
ENST00000566128.1:c.39-566T>A ENSP00000456276.1:n.39-566T>A
ENST00000569082.1:n.232-566T>A
NM_000078.2:c.234-566T>A NP_000069.2:n.234-566T>A
NM_001286085.1:c.234-566T>A NP_001273014.1:n.234-566T>A
XM_006721124.2:c.234-566T>A XP_006721187.1:n.234-566T>A
XM_006721124.3:c.234-566T>A XP_006721187.1:n.234-566T>A
NM_000078.3:c.234-566T>A MANE Select NP_000069.2:n.234-566T>A
NM_001286085.2:c.234-566T>A NP_001273014.1:n.234-566T>A