Canonical Allele Identifier: CA722015773

Gene: CETP

Linked Data

• dbSNP Id: rs1469689169
• gnomAD v3: 16-56971471-C-A
• gnomAD v4: 16-56971471-C-A
• MyVariant Identifiers: chr16:g.57005383C>A (hg19) ; chr16:g.56971471C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56971471C>A , CM000678.2:g.56971471C>A	GRCh38
NC_000016.9:g.57005383C>A , CM000678.1:g.57005383C>A	GRCh37
NC_000016.8:g.55562884C>A	NCBI36
NG_008952.1:g.14549C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.658+90C>A MANE Select	ENSP00000200676.3:n.658+90C>A
ENST00000200676.7:c.658+90C>A	ENSP00000200676.3:n.658+90C>A
ENST00000379780.6:c.658+90C>A	ENSP00000369106.2:n.658+90C>A
ENST00000566128.1:c.463+90C>A	ENSP00000456276.1:n.463+90C>A
ENST00000569082.1:n.760+90C>A
NM_000078.2:c.658+90C>A	NP_000069.2:n.658+90C>A
NM_001286085.1:c.658+90C>A	NP_001273014.1:n.658+90C>A
XM_006721124.2:c.658+90C>A	XP_006721187.1:n.658+90C>A
XM_006721124.3:c.658+90C>A	XP_006721187.1:n.658+90C>A
NM_000078.3:c.658+90C>A MANE Select	NP_000069.2:n.658+90C>A
NM_001286085.2:c.658+90C>A	NP_001273014.1:n.658+90C>A