Canonical Allele Identifier: CA2002760332
Gene: APOC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832901G= , CM000673.2:g.116832901G= GRCh38
NC_000011.9:g.116703617G= , CM000673.1:g.116703617G= GRCh37
NC_000011.8:g.116208827G= NCBI36
NG_008949.1:g.7994G=

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.*17G= MANE Select ENSP00000227667.2:n.*17G=
ENST00000227667.7:c.*17G= ENSP00000227667.2:n.*17G=
ENST00000375345.3:c.*17G= ENSP00000364494.1:n.*17G=
ENST00000630701.1:c.371G= ENSP00000486182.1:n.371G=
NM_000040.1:c.*17G= NP_000031.1:n.*17G=
NM_000040.2:c.*17G= NP_000031.1:n.*17G=
NM_000040.3:c.*17G= MANE Select NP_000031.1:n.*17G=