Canonical Allele Identifier: CA308876452
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

dbSNP Id: rs767871541
gnomAD v4: 19-44949379-T-C
MyVariant Identifiers: chr19:g.45452636T>C (hg19) chr19:g.44949379T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949379T>C , CM000681.2:g.44949379T>C GRCh38
NC_000019.9:g.45452636T>C , CM000681.1:g.45452636T>C GRCh37
NC_000019.8:g.50144476T>C NCBI36
NG_008837.1:g.8394T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.*130T>C (APOC2) MANE Select ENSP00000252490.5:n.*130T>C
ENST00000252490.5:c.*130T>C (APOC4-APOC2) ENSP00000252490.4:n.*130T>C
ENST00000585685.5:c.*1219T>C (APOC4-APOC2) ENSP00000467185.1:n.*1219T>C
ENST00000590360.2:c.*130T>C (APOC2) ENSP00000466775.1:n.*130T>C
ENST00000591597.5:c.*130T>C (APOC2) ENSP00000476835.1:n.*130T>C
ENST00000592257.5:c.*230T>C (APOC2) ENSP00000477261.1:n.*230T>C
NM_000483.4:c.*130T>C (APOC2) NP_000474.2:n.*130T>C
NR_037932.1:n.1643T>C (APOC4-APOC2)
NM_000483.5:c.*130T>C (APOC2) MANE Select NP_000474.2:n.*130T>C
Search 100 bp 5'
Search 100 bp 3'