Canonical Allele Identifier: CA308876556

Gene: APOC2 APOC4-APOC2

Linked Data

• dbSNP Id: rs186152230
• gnomAD v2: 19-45452711-T-A
• gnomAD v3: 19-44949454-T-A
• gnomAD v4: 19-44949454-T-A
• MyVariant Identifiers: chr19:g.45452711T>A (hg19) ; chr19:g.44949454T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949454T>A , CM000681.2:g.44949454T>A	GRCh38
NC_000019.9:g.45452711T>A , CM000681.1:g.45452711T>A	GRCh37
NC_000019.8:g.50144551T>A	NCBI36
NG_008837.1:g.8469T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.*205T>A (APOC2) MANE Select	ENSP00000252490.5:n.*205T>A
ENST00000252490.5:c.*205T>A (APOC4-APOC2)	ENSP00000252490.4:n.*205T>A
ENST00000585685.5:c.*1294T>A (APOC4-APOC2)	ENSP00000467185.1:n.*1294T>A
ENST00000590360.2:c.*205T>A (APOC2)	ENSP00000466775.1:n.*205T>A
NM_000483.4:c.*205T>A (APOC2)	NP_000474.2:n.*205T>A
NR_037932.1:n.1718T>A (APOC4-APOC2)
NM_000483.5:c.*205T>A (APOC2) MANE Select	NP_000474.2:n.*205T>A