Canonical Allele Identifier: CA977681134
Gene: CETP HGNC NCBI

Linked Data

dbSNP Id: rs2056202825
gnomAD v3: 16-56983436-G-C
gnomAD v4: 16-56983436-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56983436G>C , CM000678.2:g.56983436G>C GRCh38
NC_000016.9:g.57017348G>C , CM000678.1:g.57017348G>C GRCh37
NC_000016.8:g.55574849G>C NCBI36
NG_008952.1:g.26514G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000200676.8:c.1407+25G>C MANE Select ENSP00000200676.3:n.1407+25G>C
ENST00000200676.7:c.1407+25G>C ENSP00000200676.3:n.1407+25G>C
ENST00000379780.6:c.1227+25G>C ENSP00000369106.2:n.1227+25G>C
ENST00000566128.1:c.1212+25G>C ENSP00000456276.1:n.1212+25G>C
NM_000078.2:c.1407+25G>C NP_000069.2:n.1407+25G>C
NM_001286085.1:c.1227+25G>C NP_001273014.1:n.1227+25G>C
NM_000078.3:c.1407+25G>C MANE Select NP_000069.2:n.1407+25G>C
NM_001286085.2:c.1227+25G>C NP_001273014.1:n.1227+25G>C
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