Canonical Allele Identifier: CA8070714
Gene: CETP HGNC NCBI

Linked Data

dbSNP Id: rs757176551

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56961932C>G , CM000678.2:g.56961932C>G GRCh38
NC_000016.9:g.56995844C>G , CM000678.1:g.56995844C>G GRCh37
NC_000016.8:g.55553345C>G NCBI36
NG_008952.1:g.5010C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000200676.7:c.-48C>G ENSP00000200676.3:n.-48C>G
ENST00000379780.6:c.-48C>G ENSP00000369106.2:n.-48C>G
NM_000078.2:c.-48C>G NP_000069.2:n.-48C>G
NM_001286085.1:c.-48C>G NP_001273014.1:n.-48C>G