Canonical Allele Identifier: CA2002760394
Gene: APOC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116833007C= , CM000673.2:g.116833007C= GRCh38
NC_000011.9:g.116703723C= , CM000673.1:g.116703723C= GRCh37
NC_000011.8:g.116208933C= NCBI36
NG_008949.1:g.8100C=

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.*123C= MANE Select ENSP00000227667.2:n.*123C=
ENST00000227667.7:c.*123C= ENSP00000227667.2:n.*123C=
ENST00000375345.3:c.*123C= ENSP00000364494.1:n.*123C=
ENST00000630701.1:c.477C= ENSP00000486182.1:n.477C=
NM_000040.1:c.*123C= NP_000031.1:n.*123C=
NM_000040.2:c.*123C= NP_000031.1:n.*123C=
NM_000040.3:c.*123C= MANE Select NP_000031.1:n.*123C=