Canonical Allele Identifier: CA633478877
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

dbSNP Id: rs1568634972
gnomAD v2: 19-45452279-TCAGACCCAGGAGTCCAGGCCCCCAGCCCC-T
gnomAD v3: 19-44949022-TCAGACCCAGGAGTCCAGGCCCCCAGCCCC-T
gnomAD v4: 19-44949022-TCAGACCCAGGAGTCCAGGCCCCCAGCCCC-T
MyVariant Identifiers: chr19:g.45452280_45452345delinsTCCTCCCTCAGACCCAGGAGTCCAGGTCCCCAGACCC (hg19) chr19:g.44949023_44949088delinsTCCTCCCTCAGACCCAGGAGTCCAGGTCCCCAGACCC (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949023_44949051del , CM000681.2:g.44949023_44949051del GRCh38
NC_000019.9:g.45452280_45452308del , CM000681.1:g.45452280_45452308del GRCh37
NC_000019.8:g.50144120_50144148del NCBI36
NG_008837.1:g.8038_8066del

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.216-136_216-108del (APOC2) MANE Select ENSP00000252490.5:n.216-136_216-108del
ENST00000252490.5:c.216-136_216-108del (APOC4-APOC2) ENSP00000252490.4:n.216-136_216-108del
ENST00000585685.5:c.*999-136_*999-108del (APOC4-APOC2) ENSP00000467185.1:n.*999-136_*999-108del
ENST00000585786.1:c.*159_*187del (APOC2) ENSP00000465001.1:n.*159_*187del
ENST00000589057.5:c.447-136_447-108del (APOC4-APOC2) ENSP00000468139.1:n.447-136_447-108del
ENST00000590360.2:c.216-136_216-108del (APOC2) ENSP00000466775.1:n.216-136_216-108del
ENST00000591597.5:c.174-136_174-108del (APOC2) ENSP00000476835.1:n.174-136_174-108del
ENST00000592257.5:c.*10-136_*10-108del (APOC2) ENSP00000477261.1:n.*10-136_*10-108del
NM_000483.4:c.216-136_216-108del (APOC2) NP_000474.2:n.216-136_216-108del
NR_037932.1:n.1423-136_1423-108del (APOC4-APOC2)
NM_000483.5:c.216-136_216-108del (APOC2) MANE Select NP_000474.2:n.216-136_216-108del
Search 100 bp 5'
Search 100 bp 3'