Canonical Allele Identifier: CA281521306

Gene: CETP

Linked Data

• dbSNP Id: rs1004221460
• gnomAD v3: 16-56968899-T-G
• gnomAD v4: 16-56968899-T-G
• MyVariant Identifiers: chr16:g.57002811T>G (hg19) ; chr16:g.56968899T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56968899T>G , CM000678.2:g.56968899T>G	GRCh38
NC_000016.9:g.57002811T>G , CM000678.1:g.57002811T>G	GRCh37
NC_000016.8:g.55560312T>G	NCBI36
NG_008952.1:g.11977T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.234-487T>G MANE Select	ENSP00000200676.3:n.234-487T>G
ENST00000200676.7:c.234-487T>G	ENSP00000200676.3:n.234-487T>G
ENST00000379780.6:c.234-487T>G	ENSP00000369106.2:n.234-487T>G
ENST00000566128.1:c.39-487T>G	ENSP00000456276.1:n.39-487T>G
ENST00000569082.1:n.232-487T>G
NM_000078.2:c.234-487T>G	NP_000069.2:n.234-487T>G
NM_001286085.1:c.234-487T>G	NP_001273014.1:n.234-487T>G
XM_006721124.2:c.234-487T>G	XP_006721187.1:n.234-487T>G
XM_006721124.3:c.234-487T>G	XP_006721187.1:n.234-487T>G
NM_000078.3:c.234-487T>G MANE Select	NP_000069.2:n.234-487T>G
NM_001286085.2:c.234-487T>G	NP_001273014.1:n.234-487T>G