Canonical Allele Identifier: CA308876393
Community Standard Title: NM_000483.5(APOC2):c.*20T>C
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949269T>C , CM000681.2:g.44949269T>C GRCh38
NC_000019.9:g.45452526T>C , CM000681.1:g.45452526T>C GRCh37
NC_000019.8:g.50144366T>C NCBI36
NG_008837.1:g.8284T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000483.5:c.*20T>C (APOC2) MANE Select NP_000474.2:n.*20T>C
ENST00000252490.7:c.*20T>C (APOC2) MANE Select ENSP00000252490.5:n.*20T>C
NM_000483.4:c.*20T>C (APOC2) NP_000474.2:n.*20T>C
NR_037932.1:n.1533T>C (APOC4-APOC2)
ENST00000252490.5:c.*20T>C (APOC4-APOC2) ENSP00000252490.4:n.*20T>C
ENST00000585685.5:c.*1109T>C (APOC4-APOC2) ENSP00000467185.1:n.*1109T>C
ENST00000585786.1:c.*405T>C (APOC2) ENSP00000465001.1:n.*405T>C
ENST00000589057.5:c.*20T>C (APOC4-APOC2) ENSP00000468139.1:n.*20T>C
ENST00000590360.2:c.*20T>C (APOC2) ENSP00000466775.1:n.*20T>C
ENST00000591597.5:c.*20T>C (APOC2) ENSP00000476835.1:n.*20T>C
ENST00000592257.5:c.*120T>C (APOC2) ENSP00000477261.1:n.*120T>C