Canonical Allele Identifier: CA920117776
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

dbSNP Id: rs1568634965
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949016_44949017insTTC , CM000681.2:g.44949016_44949017insTTC GRCh38
NC_000019.9:g.45452273_45452274insTTC , CM000681.1:g.45452273_45452274insTTC GRCh37
NC_000019.8:g.50144113_50144114insTTC NCBI36
NG_008837.1:g.8031_8032insTTC

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.216-143_216-142insTTC (APOC2) MANE Select ENSP00000252490.5:n.216-143_216-142insTTC...
ENST00000252490.5:c.216-143_216-142insTTC (APOC4-APOC2) ENSP00000252490.4:n.216-143_216-142insTTC...
ENST00000585685.5:c.*999-143_*999-142insTTC (APOC4-APOC2) ENSP00000467185.1:n.*999-143_*999-142insT...
ENST00000585786.1:c.*152_*153insTTC (APOC2) ENSP00000465001.1:n.*152_*153insTTC
ENST00000589057.5:c.447-143_447-142insTTC (APOC4-APOC2) ENSP00000468139.1:n.447-143_447-142insTTC...
ENST00000590360.2:c.216-143_216-142insTTC (APOC2) ENSP00000466775.1:n.216-143_216-142insTTC...
ENST00000591597.5:c.174-143_174-142insTTC (APOC2) ENSP00000476835.1:n.174-143_174-142insTTC...
ENST00000592257.5:c.*10-143_*10-142insTTC (APOC2) ENSP00000477261.1:n.*10-143_*10-142insTTC...
NM_000483.4:c.216-143_216-142insTTC (APOC2) NP_000474.2:n.216-143_216-142insTTC
NR_037932.1:n.1423-143_1423-142insTTC (APOC4-APOC2)
NM_000483.5:c.216-143_216-142insTTC (APOC2) MANE Select NP_000474.2:n.216-143_216-142insTTC
Search 100 bp 5'
Search 100 bp 3'