Canonical Allele Identifier: CA722013364
Gene: CETP HGNC NCBI

Linked Data

dbSNP Id: rs1484833695

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56968967A>G , CM000678.2:g.56968967A>G GRCh38
NC_000016.9:g.57002879A>G , CM000678.1:g.57002879A>G GRCh37
NC_000016.8:g.55560380A>G NCBI36
NG_008952.1:g.12045A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000200676.8:c.234-419A>G MANE Select ENSP00000200676.3:n.234-419A>G
ENST00000200676.7:c.234-419A>G ENSP00000200676.3:n.234-419A>G
ENST00000379780.6:c.234-419A>G ENSP00000369106.2:n.234-419A>G
ENST00000566128.1:c.39-419A>G ENSP00000456276.1:n.39-419A>G
ENST00000569082.1:n.232-419A>G
NM_000078.2:c.234-419A>G NP_000069.2:n.234-419A>G
NM_001286085.1:c.234-419A>G NP_001273014.1:n.234-419A>G
XM_006721124.2:c.234-419A>G XP_006721187.1:n.234-419A>G
XM_006721124.3:c.234-419A>G XP_006721187.1:n.234-419A>G
NM_000078.3:c.234-419A>G MANE Select NP_000069.2:n.234-419A>G
NM_001286085.2:c.234-419A>G NP_001273014.1:n.234-419A>G