Canonical Allele Identifier: CA2633386153
Gene: CETP HGNC NCBI

Linked Data

gnomAD v4: 16-56971484-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56971484T>C , CM000678.2:g.56971484T>C GRCh38
NC_000016.9:g.57005396T>C , CM000678.1:g.57005396T>C GRCh37
NC_000016.8:g.55562897T>C NCBI36
NG_008952.1:g.14562T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000200676.8:c.658+103T>C MANE Select ENSP00000200676.3:n.658+103T>C
ENST00000200676.7:c.658+103T>C ENSP00000200676.3:n.658+103T>C
ENST00000379780.6:c.658+103T>C ENSP00000369106.2:n.658+103T>C
ENST00000566128.1:c.463+103T>C ENSP00000456276.1:n.463+103T>C
ENST00000569082.1:n.760+103T>C
NM_000078.2:c.658+103T>C NP_000069.2:n.658+103T>C
NM_001286085.1:c.658+103T>C NP_001273014.1:n.658+103T>C
XM_006721124.2:c.658+103T>C XP_006721187.1:n.658+103T>C
XM_006721124.3:c.658+103T>C XP_006721187.1:n.658+103T>C
NM_000078.3:c.658+103T>C MANE Select NP_000069.2:n.658+103T>C
NM_001286085.2:c.658+103T>C NP_001273014.1:n.658+103T>C
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