Canonical Allele Identifier: CA996271815
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

dbSNP Id: rs1970360772
gnomAD v3: 19-44949448-A-T
gnomAD v4: 19-44949448-A-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949448A>T , CM000681.2:g.44949448A>T GRCh38
NC_000019.9:g.45452705A>T , CM000681.1:g.45452705A>T GRCh37
NC_000019.8:g.50144545A>T NCBI36
NG_008837.1:g.8463A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.*199A>T (APOC2) MANE Select ENSP00000252490.5:n.*199A>T
ENST00000252490.5:c.*199A>T (APOC4-APOC2) ENSP00000252490.4:n.*199A>T
ENST00000585685.5:c.*1288A>T (APOC4-APOC2) ENSP00000467185.1:n.*1288A>T
ENST00000590360.2:c.*199A>T (APOC2) ENSP00000466775.1:n.*199A>T
NM_000483.4:c.*199A>T (APOC2) NP_000474.2:n.*199A>T
NR_037932.1:n.1712A>T (APOC4-APOC2)
NM_000483.5:c.*199A>T (APOC2) MANE Select NP_000474.2:n.*199A>T
Search 100 bp 5'
Search 100 bp 3'