Canonical Allele Identifier: CA281527505

Gene: CETP

Linked Data

• dbSNP Id: rs572033689
• gnomAD v3: 16-56978368-C-G
• gnomAD v4: 16-56978368-C-G
• MyVariant Identifiers: chr16:g.57012280C>G (hg19) ; chr16:g.56978368C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56978368C>G , CM000678.2:g.56978368C>G	GRCh38
NC_000016.9:g.57012280C>G , CM000678.1:g.57012280C>G	GRCh37
NC_000016.8:g.55569781C>G	NCBI36
NG_008952.1:g.21446C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.1146+113C>G MANE Select	ENSP00000200676.3:n.1146+113C>G
ENST00000650358.1:n.1544+113C>G
ENST00000200676.7:c.1146+113C>G	ENSP00000200676.3:n.1146+113C>G
ENST00000379780.6:c.966+113C>G	ENSP00000369106.2:n.966+113C>G
ENST00000566128.1:c.951+113C>G	ENSP00000456276.1:n.951+113C>G
NM_000078.2:c.1146+113C>G	NP_000069.2:n.1146+113C>G
NM_001286085.1:c.966+113C>G	NP_001273014.1:n.966+113C>G
NM_000078.3:c.1146+113C>G MANE Select	NP_000069.2:n.1146+113C>G
NM_001286085.2:c.966+113C>G	NP_001273014.1:n.966+113C>G