Canonical Allele Identifier: CA495622665

Gene: CETP

Linked Data

• dbSNP Id: rs771246247
• gnomAD v4: 16-56983402-C-T
• MyVariant Identifiers: chr16:g.57017314C>T (hg19) ; chr16:g.56983402C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56983402C>T , CM000678.2:g.56983402C>T	GRCh38
NC_000016.9:g.57017314C>T , CM000678.1:g.57017314C>T	GRCh37
NC_000016.8:g.55574815C>T	NCBI36
NG_008952.1:g.26480C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200676.8:c.1398C>T MANE Select	ENSP00000200676.3:p.Ile466=
ENST00000200676.7:c.1398C>T	ENSP00000200676.3:p.Ile466=
ENST00000379780.6:c.1218C>T	ENSP00000369106.2:p.Ile406=
ENST00000566128.1:c.1203C>T	ENSP00000456276.1:p.Ile401=
NM_000078.2:c.1398C>T	NP_000069.2:p.Ile466=
NM_001286085.1:c.1218C>T	NP_001273014.1:p.Ile406=
NM_000078.3:c.1398C>T MANE Select	NP_000069.2:p.Ile466=
NM_001286085.2:c.1218C>T	NP_001273014.1:p.Ile406=