Canonical Allele Identifier: CA2002760252
Gene: APOC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832729A= , CM000673.2:g.116832729A= GRCh38
NC_000011.9:g.116703445A= , CM000673.1:g.116703445A= GRCh37
NC_000011.8:g.116208655A= NCBI36
NG_008949.1:g.7822A=

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.180-35A= MANE Select ENSP00000227667.2:n.180-35A=
ENST00000227667.7:c.180-35A= ENSP00000227667.2:n.180-35A=
ENST00000375345.3:c.234-35A= ENSP00000364494.1:n.234-35A=
ENST00000630701.1:c.234-35A= ENSP00000486182.1:n.234-35A=
NM_000040.1:c.180-35A= NP_000031.1:n.180-35A=
NM_000040.2:c.180-35A= NP_000031.1:n.180-35A=
NM_000040.3:c.180-35A= MANE Select NP_000031.1:n.180-35A=