Canonical Allele Identifier: CA2002760299
Gene: APOC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832839G= , CM000673.2:g.116832839G= GRCh38
NC_000011.9:g.116703555G= , CM000673.1:g.116703555G= GRCh37
NC_000011.8:g.116208765G= NCBI36
NG_008949.1:g.7932G=

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.255G= MANE Select ENSP00000227667.2:p.Trp85=
ENST00000227667.7:c.255G= ENSP00000227667.2:p.Trp85=
ENST00000375345.3:c.309G= ENSP00000364494.1:p.Trp103=
ENST00000630701.1:c.309G= ENSP00000486182.1:p.Trp103=
NM_000040.1:c.255G= NP_000031.1:p.Trp85=
NM_000040.2:c.255G= NP_000031.1:p.Trp85=
NM_000040.3:c.255G= MANE Select NP_000031.1:p.Trp85=