Canonical Allele Identifier: CA722023190

Gene: CETP

Linked Data

• dbSNP Id: rs1410793346
• gnomAD v3: 16-56982086-T-C
• gnomAD v4: 16-56982086-T-C
• MyVariant Identifiers: chr16:g.57015998T>C (hg19) ; chr16:g.56982086T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56982086T>C , CM000678.2:g.56982086T>C	GRCh38
NC_000016.9:g.57015998T>C , CM000678.1:g.57015998T>C	GRCh37
NC_000016.8:g.55573499T>C	NCBI36
NG_008952.1:g.25164T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000200676.8:c.1249-79T>C MANE Select	ENSP00000200676.3:n.1249-79T>C
ENST00000650358.1:n.1647-79T>C
ENST00000200676.7:c.1249-79T>C	ENSP00000200676.3:n.1249-79T>C
ENST00000379780.6:c.1069-79T>C	ENSP00000369106.2:n.1069-79T>C
ENST00000566128.1:c.1054-79T>C	ENSP00000456276.1:n.1054-79T>C
NM_000078.2:c.1249-79T>C	NP_000069.2:n.1249-79T>C
NM_001286085.1:c.1069-79T>C	NP_001273014.1:n.1069-79T>C
NM_000078.3:c.1249-79T>C MANE Select	NP_000069.2:n.1249-79T>C
NM_001286085.2:c.1069-79T>C	NP_001273014.1:n.1069-79T>C