Canonical Allele Identifier: CA633312203
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

dbSNP Id: rs1452412987
gnomAD v2: 19-45452709-GC-G
gnomAD v3: 19-44949452-GC-G
gnomAD v4: 19-44949452-GC-G
MyVariant Identifiers: chr19:g.45452710del (hg19) chr19:g.44949453del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949453del , CM000681.2:g.44949453del GRCh38
NC_000019.9:g.45452710del , CM000681.1:g.45452710del GRCh37
NC_000019.8:g.50144550del NCBI36
NG_008837.1:g.8468del

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.*204del (APOC2) MANE Select ENSP00000252490.5:n.*204del
ENST00000252490.5:c.*204del (APOC4-APOC2) ENSP00000252490.4:n.*204del
ENST00000585685.5:c.*1293del (APOC4-APOC2) ENSP00000467185.1:n.*1293del
ENST00000590360.2:c.*204del (APOC2) ENSP00000466775.1:n.*204del
NM_000483.4:c.*204del (APOC2) NP_000474.2:n.*204del
NR_037932.1:n.1717del (APOC4-APOC2)
NM_000483.5:c.*204del (APOC2) MANE Select NP_000474.2:n.*204del
Search 100 bp 5'
Search 100 bp 3'