Canonical Allele Identifier: CA10652059
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 329457
ClinVar RCV Id: RCV000362575 RCV001559958
dbSNP Id: rs7253690
gnomAD v2: 19-45452596-C-T
gnomAD v3: 19-44949339-C-T
gnomAD v4: 19-44949339-C-T
MyVariant Identifiers: chr19:g.45452596C>T (hg19) chr19:g.44949339C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949339C>T , CM000681.2:g.44949339C>T GRCh38
NC_000019.9:g.45452596C>T , CM000681.1:g.45452596C>T GRCh37
NC_000019.8:g.50144436C>T NCBI36
NG_008837.1:g.8354C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.*90C>T (APOC2) MANE Select ENSP00000252490.5:n.*90C>T
ENST00000252490.5:c.*90C>T (APOC4-APOC2) ENSP00000252490.4:n.*90C>T
ENST00000585685.5:c.*1179C>T (APOC4-APOC2) ENSP00000467185.1:n.*1179C>T
ENST00000589057.5:c.*90C>T (APOC4-APOC2) ENSP00000468139.1:n.*90C>T
ENST00000590360.2:c.*90C>T (APOC2) ENSP00000466775.1:n.*90C>T
ENST00000591597.5:c.*90C>T (APOC2) ENSP00000476835.1:n.*90C>T
ENST00000592257.5:c.*190C>T (APOC2) ENSP00000477261.1:n.*190C>T
NM_000483.4:c.*90C>T (APOC2) NP_000474.2:n.*90C>T
NR_037932.1:n.1603C>T (APOC4-APOC2)
NM_000483.5:c.*90C>T (APOC2) MANE Select NP_000474.2:n.*90C>T
Search 100 bp 5'
Search 100 bp 3'