Canonical Allele Identifier: CA2633385719
Gene: CETP HGNC NCBI

Linked Data

gnomAD v4: 16-56978367-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56978367G>C , CM000678.2:g.56978367G>C GRCh38
NC_000016.9:g.57012279G>C , CM000678.1:g.57012279G>C GRCh37
NC_000016.8:g.55569780G>C NCBI36
NG_008952.1:g.21445G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000200676.8:c.1146+112G>C MANE Select ENSP00000200676.3:n.1146+112G>C
ENST00000650358.1:n.1544+112G>C
ENST00000200676.7:c.1146+112G>C ENSP00000200676.3:n.1146+112G>C
ENST00000379780.6:c.966+112G>C ENSP00000369106.2:n.966+112G>C
ENST00000566128.1:c.951+112G>C ENSP00000456276.1:n.951+112G>C
NM_000078.2:c.1146+112G>C NP_000069.2:n.1146+112G>C
NM_001286085.1:c.966+112G>C NP_001273014.1:n.966+112G>C
NM_000078.3:c.1146+112G>C MANE Select NP_000069.2:n.1146+112G>C
NM_001286085.2:c.966+112G>C NP_001273014.1:n.966+112G>C
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