Canonical Allele Identifier: CA281523045
Gene: CETP HGNC NCBI

Linked Data

dbSNP Id: rs535464315
gnomAD v2: 16-57005496-G-A
gnomAD v3: 16-56971584-G-A
gnomAD v4: 16-56971584-G-A
MyVariant Identifiers: chr16:g.57005496G>A (hg19) chr16:g.56971584G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56971584G>A , CM000678.2:g.56971584G>A GRCh38
NC_000016.9:g.57005496G>A , CM000678.1:g.57005496G>A GRCh37
NC_000016.8:g.55562997G>A NCBI36
NG_008952.1:g.14662G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000200676.8:c.658+203G>A MANE Select ENSP00000200676.3:n.658+203G>A
ENST00000200676.7:c.658+203G>A ENSP00000200676.3:n.658+203G>A
ENST00000379780.6:c.658+203G>A ENSP00000369106.2:n.658+203G>A
ENST00000566128.1:c.463+203G>A ENSP00000456276.1:n.463+203G>A
ENST00000569082.1:n.760+203G>A
NM_000078.2:c.658+203G>A NP_000069.2:n.658+203G>A
NM_001286085.1:c.658+203G>A NP_001273014.1:n.658+203G>A
XM_006721124.2:c.658+203G>A XP_006721187.1:n.658+203G>A
XM_006721124.3:c.658+203G>A XP_006721187.1:n.658+203G>A
NM_000078.3:c.658+203G>A MANE Select NP_000069.2:n.658+203G>A
NM_001286085.2:c.658+203G>A NP_001273014.1:n.658+203G>A
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