Canonical Allele Identifier: CA2224402579
Gene: CETP HGNC NCBI

Linked Data

dbSNP Id: rs1597009030
gnomAD v4: 16-56983432-A-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56983432A>C , CM000678.2:g.56983432A>C GRCh38
NC_000016.9:g.57017344A>C , CM000678.1:g.57017344A>C GRCh37
NC_000016.8:g.55574845A>C NCBI36
NG_008952.1:g.26510A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000200676.8:c.1407+21A>C MANE Select ENSP00000200676.3:n.1407+21A>C
ENST00000200676.7:c.1407+21A>C ENSP00000200676.3:n.1407+21A>C
ENST00000379780.6:c.1227+21A>C ENSP00000369106.2:n.1227+21A>C
ENST00000566128.1:c.1212+21A>C ENSP00000456276.1:n.1212+21A>C
NM_000078.2:c.1407+21A>C NP_000069.2:n.1407+21A>C
NM_001286085.1:c.1227+21A>C NP_001273014.1:n.1227+21A>C
NM_000078.3:c.1407+21A>C MANE Select NP_000069.2:n.1407+21A>C
NM_001286085.2:c.1227+21A>C NP_001273014.1:n.1227+21A>C
Search 100 bp 5'
Search 100 bp 3'