Canonical Allele Identifier: CA2338188999
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949439C= , CM000681.2:g.44949439C= GRCh38
NC_000019.9:g.45452696C= , CM000681.1:g.45452696C= GRCh37
NC_000019.8:g.50144536C= NCBI36
NG_008837.1:g.8454C=

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.*190C= (APOC2) MANE Select ENSP00000252490.5:n.*190C=
ENST00000252490.5:c.*190C= (APOC4-APOC2) ENSP00000252490.4:n.*190C=
ENST00000585685.5:c.*1279C= (APOC4-APOC2) ENSP00000467185.1:n.*1279C=
ENST00000590360.2:c.*190C= (APOC2) ENSP00000466775.1:n.*190C=
NM_000483.4:c.*190C= (APOC2) NP_000474.2:n.*190C=
NR_037932.1:n.1703C= (APOC4-APOC2)
NM_000483.5:c.*190C= (APOC2) MANE Select NP_000474.2:n.*190C=