Canonical Allele Identifier: CA722016677

Gene: CETP

Linked Data

• dbSNP Id: rs7499892
• MyVariant Identifiers: chr16:g.57006590C>G (hg19) ; chr16:g.56972678C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56972678C>G , CM000678.2:g.56972678C>G	GRCh38
NC_000016.9:g.57006590C>G , CM000678.1:g.57006590C>G	GRCh37
NC_000016.8:g.55564091C>G	NCBI36
NG_008952.1:g.15756C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.750+595C>G MANE Select	ENSP00000200676.3:n.750+595C>G
ENST00000200676.7:c.750+595C>G	ENSP00000200676.3:n.750+595C>G
ENST00000379780.6:c.750+595C>G	ENSP00000369106.2:n.750+595C>G
ENST00000566128.1:c.555+595C>G	ENSP00000456276.1:n.555+595C>G
ENST00000569082.1:n.852+595C>G
NM_000078.2:c.750+595C>G	NP_000069.2:n.750+595C>G
NM_001286085.1:c.750+595C>G	NP_001273014.1:n.750+595C>G
XM_006721124.2:c.*459C>G	XP_006721187.1:n.*459C>G
XM_006721124.3:c.*459C>G	XP_006721187.1:n.*459C>G
NM_000078.3:c.750+595C>G MANE Select	NP_000069.2:n.750+595C>G
NM_001286085.2:c.750+595C>G	NP_001273014.1:n.750+595C>G