Canonical Allele Identifier: CA2585725219
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

gnomAD v4: 19-44949445-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949445T>C , CM000681.2:g.44949445T>C GRCh38
NC_000019.9:g.45452702T>C , CM000681.1:g.45452702T>C GRCh37
NC_000019.8:g.50144542T>C NCBI36
NG_008837.1:g.8460T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.*196T>C (APOC2) MANE Select ENSP00000252490.5:n.*196T>C
ENST00000252490.5:c.*196T>C (APOC4-APOC2) ENSP00000252490.4:n.*196T>C
ENST00000585685.5:c.*1285T>C (APOC4-APOC2) ENSP00000467185.1:n.*1285T>C
ENST00000590360.2:c.*196T>C (APOC2) ENSP00000466775.1:n.*196T>C
NM_000483.4:c.*196T>C (APOC2) NP_000474.2:n.*196T>C
NR_037932.1:n.1709T>C (APOC4-APOC2)
NM_000483.5:c.*196T>C (APOC2) MANE Select NP_000474.2:n.*196T>C
Search 100 bp 5'
Search 100 bp 3'