Canonical Allele Identifier: CA14266406
Gene: CETP HGNC NCBI

Linked Data

dbSNP Id: rs9939224

Genomic Alleles

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

Transcript Alleles

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