Canonical Allele Identifier: CA722023124
Gene: CETP HGNC NCBI

Linked Data

dbSNP Id: rs1244254216
MyVariant Identifiers: chr16:g.57015916C>G (hg19) chr16:g.56982004C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56982004C>G , CM000678.2:g.56982004C>G GRCh38
NC_000016.9:g.57015916C>G , CM000678.1:g.57015916C>G GRCh37
NC_000016.8:g.55573417C>G NCBI36
NG_008952.1:g.25082C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000200676.8:c.1249-161C>G MANE Select ENSP00000200676.3:n.1249-161C>G
ENST00000650358.1:n.1647-161C>G
ENST00000200676.7:c.1249-161C>G ENSP00000200676.3:n.1249-161C>G
ENST00000379780.6:c.1069-161C>G ENSP00000369106.2:n.1069-161C>G
ENST00000566128.1:c.1054-161C>G ENSP00000456276.1:n.1054-161C>G
NM_000078.2:c.1249-161C>G NP_000069.2:n.1249-161C>G
NM_001286085.1:c.1069-161C>G NP_001273014.1:n.1069-161C>G
NM_000078.3:c.1249-161C>G MANE Select NP_000069.2:n.1249-161C>G
NM_001286085.2:c.1069-161C>G NP_001273014.1:n.1069-161C>G
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