Canonical Allele Identifier: CA656558761

Gene: CETP

Linked Data

• dbSNP Id: rs1452131839
• gnomAD v3: 16-56968793-C-T
• gnomAD v4: 16-56968793-C-T
• COSMIC: COSN17535860
• MyVariant Identifiers: chr16:g.57002705C>T (hg19) ; chr16:g.56968793C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56968793C>T , CM000678.2:g.56968793C>T	GRCh38
NC_000016.9:g.57002705C>T , CM000678.1:g.57002705C>T	GRCh37
NC_000016.8:g.55560206C>T	NCBI36
NG_008952.1:g.11871C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.234-593C>T MANE Select	ENSP00000200676.3:n.234-593C>T
ENST00000200676.7:c.234-593C>T	ENSP00000200676.3:n.234-593C>T
ENST00000379780.6:c.234-593C>T	ENSP00000369106.2:n.234-593C>T
ENST00000566128.1:c.39-593C>T	ENSP00000456276.1:n.39-593C>T
ENST00000569082.1:n.232-593C>T
NM_000078.2:c.234-593C>T	NP_000069.2:n.234-593C>T
NM_001286085.1:c.234-593C>T	NP_001273014.1:n.234-593C>T
XM_006721124.2:c.234-593C>T	XP_006721187.1:n.234-593C>T
XM_006721124.3:c.234-593C>T	XP_006721187.1:n.234-593C>T
NM_000078.3:c.234-593C>T MANE Select	NP_000069.2:n.234-593C>T
NM_001286085.2:c.234-593C>T	NP_001273014.1:n.234-593C>T