Canonical Allele Identifier: CA406291879
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44948519T>G , CM000681.2:g.44948519T>G GRCh38
NC_000019.9:g.45451776T>G , CM000681.1:g.45451776T>G GRCh37
NC_000019.8:g.50143616T>G NCBI36
NG_008837.1:g.7534T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252490.7:c.41T>G (APOC2) MANE Select ENSP00000252490.5:p.Leu14Arg
ENST00000252490.5:c.41T>G (APOC4-APOC2) ENSP00000252490.4:p.Leu14Arg
ENST00000585685.5:c.*824T>G (APOC4-APOC2) ENSP00000467185.1:n.*824T>G
ENST00000585786.1:c.41T>G (APOC2) ENSP00000465001.1:p.Leu14Arg
ENST00000589057.5:c.272T>G (APOC4-APOC2) ENSP00000468139.1:p.Leu91Arg
ENST00000590360.2:c.41T>G (APOC2) ENSP00000466775.1:p.Leu14Arg
ENST00000591597.5:c.41T>G (APOC2) ENSP00000476835.1:p.Leu14Arg
ENST00000592257.5:c.41T>G (APOC2) ENSP00000477261.1:p.Leu14Arg
NM_000483.4:c.41T>G (APOC2) NP_000474.2:p.Leu14Arg
NR_037932.1:n.1248T>G (APOC4-APOC2)
NM_000483.5:c.41T>G (APOC2) MANE Select NP_000474.2:p.Leu14Arg