Canonical Allele Identifier: CA308876539
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

dbSNP Id: rs5127
gnomAD v4: 19-44949437-G-T
MyVariant Identifiers: chr19:g.45452694G>T (hg19) chr19:g.44949437G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949437G>T , CM000681.2:g.44949437G>T GRCh38
NC_000019.9:g.45452694G>T , CM000681.1:g.45452694G>T GRCh37
NC_000019.8:g.50144534G>T NCBI36
NG_008837.1:g.8452G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.*188G>T (APOC2) MANE Select ENSP00000252490.5:n.*188G>T
ENST00000252490.5:c.*188G>T (APOC4-APOC2) ENSP00000252490.4:n.*188G>T
ENST00000585685.5:c.*1277G>T (APOC4-APOC2) ENSP00000467185.1:n.*1277G>T
ENST00000590360.2:c.*188G>T (APOC2) ENSP00000466775.1:n.*188G>T
NM_000483.4:c.*188G>T (APOC2) NP_000474.2:n.*188G>T
NR_037932.1:n.1701G>T (APOC4-APOC2)
NM_000483.5:c.*188G>T (APOC2) MANE Select NP_000474.2:n.*188G>T
Search 100 bp 5'
Search 100 bp 3'