Canonical Allele Identifier: CA8071374
Gene: CETP HGNC NCBI

Linked Data

ClinVar Variation Id: 1476823
ClinVar RCV Id: RCV001978135
dbSNP Id: rs771246247
ExAC: 16:57017314 C / G
gnomAD v2: 16-57017314-C-G
gnomAD v3: 16-56983402-C-G
gnomAD v4: 16-56983402-C-G
MyVariant Identifiers: chr16:g.57017314C>G (hg19) chr16:g.56983402C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56983402C>G , CM000678.2:g.56983402C>G GRCh38
NC_000016.9:g.57017314C>G , CM000678.1:g.57017314C>G GRCh37
NC_000016.8:g.55574815C>G NCBI36
NG_008952.1:g.26480C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000200676.8:c.1398C>G MANE Select ENSP00000200676.3:p.Ile466Met
ENST00000200676.7:c.1398C>G ENSP00000200676.3:p.Ile466Met
ENST00000379780.6:c.1218C>G ENSP00000369106.2:p.Ile406Met
ENST00000566128.1:c.1203C>G ENSP00000456276.1:p.Ile401Met
NM_000078.2:c.1398C>G NP_000069.2:p.Ile466Met
NM_001286085.1:c.1218C>G NP_001273014.1:p.Ile406Met
NM_000078.3:c.1398C>G MANE Select NP_000069.2:p.Ile466Met
NM_001286085.2:c.1218C>G NP_001273014.1:p.Ile406Met
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