Canonical Allele Identifier: CA281530090

Gene: CETP

Linked Data

• dbSNP Id: rs375723835
• gnomAD v3: 16-56983425-C-T
• gnomAD v4: 16-56983425-C-T
• MyVariant Identifiers: chr16:g.57017337C>T (hg19) ; chr16:g.56983425C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56983425C>T , CM000678.2:g.56983425C>T	GRCh38
NC_000016.9:g.57017337C>T , CM000678.1:g.57017337C>T	GRCh37
NC_000016.8:g.55574838C>T	NCBI36
NG_008952.1:g.26503C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200676.8:c.1407+14C>T MANE Select	ENSP00000200676.3:n.1407+14C>T
ENST00000200676.7:c.1407+14C>T	ENSP00000200676.3:n.1407+14C>T
ENST00000379780.6:c.1227+14C>T	ENSP00000369106.2:n.1227+14C>T
ENST00000566128.1:c.1212+14C>T	ENSP00000456276.1:n.1212+14C>T
NM_000078.2:c.1407+14C>T	NP_000069.2:n.1407+14C>T
NM_001286085.1:c.1227+14C>T	NP_001273014.1:n.1227+14C>T
NM_000078.3:c.1407+14C>T MANE Select	NP_000069.2:n.1407+14C>T
NM_001286085.2:c.1227+14C>T	NP_001273014.1:n.1227+14C>T