Canonical Allele Identifier: CA396004119
Gene: CETP HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.57009035T>A (hg19) chr16:g.56975123T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56975123T>A , CM000678.2:g.56975123T>A GRCh38
NC_000016.9:g.57009035T>A , CM000678.1:g.57009035T>A GRCh37
NC_000016.8:g.55566536T>A NCBI36
NG_008952.1:g.18201T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000200676.8:c.953T>A MANE Select ENSP00000200676.3:p.Phe318Tyr
ENST00000200676.7:c.953T>A ENSP00000200676.3:p.Phe318Tyr
ENST00000379780.6:c.773T>A ENSP00000369106.2:p.Phe258Tyr
ENST00000566128.1:c.758T>A ENSP00000456276.1:p.Phe253Tyr
NM_000078.2:c.953T>A NP_000069.2:p.Phe318Tyr
NM_001286085.1:c.773T>A NP_001273014.1:p.Phe258Tyr
NM_000078.3:c.953T>A MANE Select NP_000069.2:p.Phe318Tyr
NM_001286085.2:c.773T>A NP_001273014.1:p.Phe258Tyr
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