Canonical Allele Identifier: CA406295217
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949184G>T , CM000681.2:g.44949184G>T GRCh38
NC_000019.9:g.45452441G>T , CM000681.1:g.45452441G>T GRCh37
NC_000019.8:g.50144281G>T NCBI36
NG_008837.1:g.8199G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.241G>T (APOC2) MANE Select ENSP00000252490.5:p.Ala81Ser
ENST00000252490.5:c.241G>T (APOC4-APOC2) ENSP00000252490.4:p.Ala81Ser
ENST00000585685.5:c.*1024G>T (APOC4-APOC2) ENSP00000467185.1:n.*1024G>T
ENST00000585786.1:c.*320G>T (APOC2) ENSP00000465001.1:n.*320G>T
ENST00000589057.5:c.472G>T (APOC4-APOC2) ENSP00000468139.1:p.Ala158Ser
ENST00000590360.2:c.241G>T (APOC2) ENSP00000466775.1:p.Ala81Ser
ENST00000591597.5:c.199G>T (APOC2) ENSP00000476835.1:p.Ala67Ser
ENST00000592257.5:c.*35G>T (APOC2) ENSP00000477261.1:n.*35G>T
NM_000483.4:c.241G>T (APOC2) NP_000474.2:p.Ala81Ser
NR_037932.1:n.1448G>T (APOC4-APOC2)
NM_000483.5:c.241G>T (APOC2) MANE Select NP_000474.2:p.Ala81Ser