Canonical Allele Identifier: CA2002758823
Gene: APOC3 HGNC NCBI

Linked Data

dbSNP Id: rs763816050
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116830652G>A , CM000673.2:g.116830652G>A GRCh38
NC_000011.9:g.116701368G>A , CM000673.1:g.116701368G>A GRCh37
NC_000011.8:g.116206578G>A NCBI36
NG_008949.1:g.5745G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.55+15G>A MANE Select ENSP00000227667.2:n.55+15G>A
ENST00000227667.7:c.55+15G>A ENSP00000227667.2:n.55+15G>A
ENST00000375345.3:c.109+15G>A ENSP00000364494.1:n.109+15G>A
ENST00000433777.5:c.55+15G>A ENSP00000410614.1:n.55+15G>A
ENST00000470144.1:n.87+15G>A
ENST00000630701.1:c.109+15G>A ENSP00000486182.1:n.109+15G>A
NM_000040.1:c.55+15G>A NP_000031.1:n.55+15G>A
NM_000040.2:c.55+15G>A NP_000031.1:n.55+15G>A
NM_000040.3:c.55+15G>A MANE Select NP_000031.1:n.55+15G>A
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