Canonical Allele Identifier: CA2002760344
Gene: APOC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832916C= , CM000673.2:g.116832916C= GRCh38
NC_000011.9:g.116703632C= , CM000673.1:g.116703632C= GRCh37
NC_000011.8:g.116208842C= NCBI36
NG_008949.1:g.8009C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.*32C= MANE Select ENSP00000227667.2:n.*32C=
ENST00000227667.7:c.*32C= ENSP00000227667.2:n.*32C=
ENST00000375345.3:c.*32C= ENSP00000364494.1:n.*32C=
ENST00000630701.1:c.386C= ENSP00000486182.1:n.386C=
NM_000040.1:c.*32C= NP_000031.1:n.*32C=
NM_000040.2:c.*32C= NP_000031.1:n.*32C=
NM_000040.3:c.*32C= MANE Select NP_000031.1:n.*32C=