Canonical Allele Identifier: CA2633388282
Gene: CETP HGNC NCBI

Linked Data

gnomAD v4: 16-56983313-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56983313T>C , CM000678.2:g.56983313T>C GRCh38
NC_000016.9:g.57017225T>C , CM000678.1:g.57017225T>C GRCh37
NC_000016.8:g.55574726T>C NCBI36
NG_008952.1:g.26391T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000200676.8:c.1322-13T>C MANE Select ENSP00000200676.3:n.1322-13T>C
ENST00000650358.1:n.1720-13T>C
ENST00000200676.7:c.1322-13T>C ENSP00000200676.3:n.1322-13T>C
ENST00000379780.6:c.1142-13T>C ENSP00000369106.2:n.1142-13T>C
ENST00000566128.1:c.1127-13T>C ENSP00000456276.1:n.1127-13T>C
NM_000078.2:c.1322-13T>C NP_000069.2:n.1322-13T>C
NM_001286085.1:c.1142-13T>C NP_001273014.1:n.1142-13T>C
NM_000078.3:c.1322-13T>C MANE Select NP_000069.2:n.1322-13T>C
NM_001286085.2:c.1142-13T>C NP_001273014.1:n.1142-13T>C
Search 100 bp 5'
Search 100 bp 3'