Canonical Allele Identifier: CA722023201

Gene: CETP

Linked Data

• dbSNP Id: rs35172227
• gnomAD v4: 16-56982095-C-A
• MyVariant Identifiers: chr16:g.57016007C>A (hg19) ; chr16:g.56982095C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56982095C>A , CM000678.2:g.56982095C>A	GRCh38
NC_000016.9:g.57016007C>A , CM000678.1:g.57016007C>A	GRCh37
NC_000016.8:g.55573508C>A	NCBI36
NG_008952.1:g.25173C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.1249-70C>A MANE Select	ENSP00000200676.3:n.1249-70C>A
ENST00000650358.1:n.1647-70C>A
ENST00000200676.7:c.1249-70C>A	ENSP00000200676.3:n.1249-70C>A
ENST00000379780.6:c.1069-70C>A	ENSP00000369106.2:n.1069-70C>A
ENST00000566128.1:c.1054-70C>A	ENSP00000456276.1:n.1054-70C>A
NM_000078.2:c.1249-70C>A	NP_000069.2:n.1249-70C>A
NM_001286085.1:c.1069-70C>A	NP_001273014.1:n.1069-70C>A
NM_000078.3:c.1249-70C>A MANE Select	NP_000069.2:n.1249-70C>A
NM_001286085.2:c.1069-70C>A	NP_001273014.1:n.1069-70C>A