Canonical Allele Identifier: CA2002760382
Gene: APOC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832991G= , CM000673.2:g.116832991G= GRCh38
NC_000011.9:g.116703707G= , CM000673.1:g.116703707G= GRCh37
NC_000011.8:g.116208917G= NCBI36
NG_008949.1:g.8084G=

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.*107G= MANE Select ENSP00000227667.2:n.*107G=
ENST00000227667.7:c.*107G= ENSP00000227667.2:n.*107G=
ENST00000375345.3:c.*107G= ENSP00000364494.1:n.*107G=
ENST00000630701.1:c.461G= ENSP00000486182.1:n.461G=
NM_000040.1:c.*107G= NP_000031.1:n.*107G=
NM_000040.2:c.*107G= NP_000031.1:n.*107G=
NM_000040.3:c.*107G= MANE Select NP_000031.1:n.*107G=