Canonical Allele Identifier: CA2338189010
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

dbSNP Id: rs1970360965

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949465A>G , CM000681.2:g.44949465A>G GRCh38
NC_000019.9:g.45452722A>G , CM000681.1:g.45452722A>G GRCh37
NC_000019.8:g.50144562A>G NCBI36
NG_008837.1:g.8480A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252490.7:c.*216A>G (APOC2) MANE Select ENSP00000252490.5:n.*216A>G
ENST00000252490.5:c.*216A>G (APOC4-APOC2) ENSP00000252490.4:n.*216A>G
ENST00000585685.5:c.*1305A>G (APOC4-APOC2) ENSP00000467185.1:n.*1305A>G
ENST00000590360.2:c.*216A>G (APOC2) ENSP00000466775.1:n.*216A>G
NM_000483.4:c.*216A>G (APOC2) NP_000474.2:n.*216A>G
NR_037932.1:n.1729A>G (APOC4-APOC2)
NM_000483.5:c.*216A>G (APOC2) MANE Select NP_000474.2:n.*216A>G