Canonical Allele Identifier: CA882680150
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

dbSNP Id: rs1337063651
gnomAD v3: 19-44949371-C-A
gnomAD v4: 19-44949371-C-A
MyVariant Identifiers: chr19:g.45452628C>A (hg19) chr19:g.44949371C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949371C>A , CM000681.2:g.44949371C>A GRCh38
NC_000019.9:g.45452628C>A , CM000681.1:g.45452628C>A GRCh37
NC_000019.8:g.50144468C>A NCBI36
NG_008837.1:g.8386C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252490.7:c.*122C>A (APOC2) MANE Select ENSP00000252490.5:n.*122C>A
ENST00000252490.5:c.*122C>A (APOC4-APOC2) ENSP00000252490.4:n.*122C>A
ENST00000585685.5:c.*1211C>A (APOC4-APOC2) ENSP00000467185.1:n.*1211C>A
ENST00000590360.2:c.*122C>A (APOC2) ENSP00000466775.1:n.*122C>A
ENST00000591597.5:c.*122C>A (APOC2) ENSP00000476835.1:n.*122C>A
ENST00000592257.5:c.*222C>A (APOC2) ENSP00000477261.1:n.*222C>A
NM_000483.4:c.*122C>A (APOC2) NP_000474.2:n.*122C>A
NR_037932.1:n.1635C>A (APOC4-APOC2)
NM_000483.5:c.*122C>A (APOC2) MANE Select NP_000474.2:n.*122C>A
Search 100 bp 5'
Search 100 bp 3'