Canonical Allele Identifier: CA2002758862
Gene: APOC3 HGNC NCBI

Linked Data

dbSNP Id: rs1941436750
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116830717_116830724del , CM000673.2:g.116830717_116830724del GRCh38
NC_000011.9:g.116701433_116701440del , CM000673.1:g.116701433_116701440del GRCh37
NC_000011.8:g.116206643_116206650del NCBI36
NG_008949.1:g.5810_5817del

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.56-56_56-49del MANE Select ENSP00000227667.2:n.56-56_56-49del
ENST00000227667.7:c.56-56_56-49del ENSP00000227667.2:n.56-56_56-49del
ENST00000375345.3:c.110-56_110-49del ENSP00000364494.1:n.110-56_110-49del
ENST00000433777.5:c.56-56_56-49del ENSP00000410614.1:n.56-56_56-49del
ENST00000470144.1:n.88-56_88-49del
ENST00000630701.1:c.110-56_110-49del ENSP00000486182.1:n.110-56_110-49del
NM_000040.1:c.56-56_56-49del NP_000031.1:n.56-56_56-49del
NM_000040.2:c.56-56_56-49del NP_000031.1:n.56-56_56-49del
NM_000040.3:c.56-56_56-49del MANE Select NP_000031.1:n.56-56_56-49del
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