Canonical Allele Identifier: CA2224401980
Gene: CETP HGNC NCBI

Linked Data

dbSNP Id: rs2056192373

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56982099C>T , CM000678.2:g.56982099C>T GRCh38
NC_000016.9:g.57016011C>T , CM000678.1:g.57016011C>T GRCh37
NC_000016.8:g.55573512C>T NCBI36
NG_008952.1:g.25177C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000200676.8:c.1249-66C>T MANE Select ENSP00000200676.3:n.1249-66C>T
ENST00000650358.1:n.1647-66C>T
ENST00000200676.7:c.1249-66C>T ENSP00000200676.3:n.1249-66C>T
ENST00000379780.6:c.1069-66C>T ENSP00000369106.2:n.1069-66C>T
ENST00000566128.1:c.1054-66C>T ENSP00000456276.1:n.1054-66C>T
NM_000078.2:c.1249-66C>T NP_000069.2:n.1249-66C>T
NM_001286085.1:c.1069-66C>T NP_001273014.1:n.1069-66C>T
NM_000078.3:c.1249-66C>T MANE Select NP_000069.2:n.1249-66C>T
NM_001286085.2:c.1069-66C>T NP_001273014.1:n.1069-66C>T