Canonical Allele Identifier: CA722012794

Gene: CETP

Linked Data

• dbSNP Id: rs867278939
• gnomAD v3: 16-56968693-G-C
• gnomAD v4: 16-56968693-G-C
• MyVariant Identifiers: chr16:g.57002605G>C (hg19) ; chr16:g.56968693G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56968693G>C , CM000678.2:g.56968693G>C	GRCh38
NC_000016.9:g.57002605G>C , CM000678.1:g.57002605G>C	GRCh37
NC_000016.8:g.55560106G>C	NCBI36
NG_008952.1:g.11771G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200676.8:c.234-693G>C MANE Select	ENSP00000200676.3:n.234-693G>C
ENST00000200676.7:c.234-693G>C	ENSP00000200676.3:n.234-693G>C
ENST00000379780.6:c.234-693G>C	ENSP00000369106.2:n.234-693G>C
ENST00000566128.1:c.39-693G>C	ENSP00000456276.1:n.39-693G>C
ENST00000569082.1:n.232-693G>C
NM_000078.2:c.234-693G>C	NP_000069.2:n.234-693G>C
NM_001286085.1:c.234-693G>C	NP_001273014.1:n.234-693G>C
XM_006721124.2:c.234-693G>C	XP_006721187.1:n.234-693G>C
XM_006721124.3:c.234-693G>C	XP_006721187.1:n.234-693G>C
NM_000078.3:c.234-693G>C MANE Select	NP_000069.2:n.234-693G>C
NM_001286085.2:c.234-693G>C	NP_001273014.1:n.234-693G>C