Canonical Allele Identifier: CA722011017
Gene: CETP HGNC NCBI

Linked Data

dbSNP Id: rs1315061250
gnomAD v3: 16-56983493-T-G
gnomAD v4: 16-56983493-T-G
MyVariant Identifiers: chr16:g.57017405T>G (hg19) chr16:g.56983493T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56983493T>G , CM000678.2:g.56983493T>G GRCh38
NC_000016.9:g.57017405T>G , CM000678.1:g.57017405T>G GRCh37
NC_000016.8:g.55574906T>G NCBI36
NG_008952.1:g.26571T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000200676.8:c.1407+82T>G MANE Select ENSP00000200676.3:n.1407+82T>G
ENST00000200676.7:c.1407+82T>G ENSP00000200676.3:n.1407+82T>G
ENST00000379780.6:c.1227+82T>G ENSP00000369106.2:n.1227+82T>G
ENST00000566128.1:c.1212+82T>G ENSP00000456276.1:n.1212+82T>G
NM_000078.2:c.1407+82T>G NP_000069.2:n.1407+82T>G
NM_001286085.1:c.1227+82T>G NP_001273014.1:n.1227+82T>G
NM_000078.3:c.1407+82T>G MANE Select NP_000069.2:n.1407+82T>G
NM_001286085.2:c.1227+82T>G NP_001273014.1:n.1227+82T>G
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