Canonical Allele Identifier: CA9506623

Gene: APOC2 APOC4-APOC2

Linked Data

• dbSNP Id: rs771464520
• ExAC: 19:45452138 A / T
• gnomAD v2: 19-45452138-A-T
• gnomAD v4: 19-44948881-A-T
• MyVariant Identifiers: chr19:g.45452138A>T (hg19) ; chr19:g.44948881A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948881A>T , CM000681.2:g.44948881A>T	GRCh38
NC_000019.9:g.45452138A>T , CM000681.1:g.45452138A>T	GRCh37
NC_000019.8:g.50143978A>T	NCBI36
NG_008837.1:g.7896A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.215+21A>T (APOC2) MANE Select	ENSP00000252490.5:n.215+21A>T
ENST00000252490.5:c.215+21A>T (APOC4-APOC2)	ENSP00000252490.4:n.215+21A>T
ENST00000585685.5:c.*998+21A>T (APOC4-APOC2)	ENSP00000467185.1:n.*998+21A>T
ENST00000585786.1:c.*17A>T (APOC2)	ENSP00000465001.1:n.*17A>T
ENST00000589057.5:c.446+21A>T (APOC4-APOC2)	ENSP00000468139.1:n.446+21A>T
ENST00000590360.2:c.215+21A>T (APOC2)	ENSP00000466775.1:n.215+21A>T
ENST00000591597.5:c.173+63A>T (APOC2)	ENSP00000476835.1:n.173+63A>T
ENST00000592257.5:c.*9+21A>T (APOC2)	ENSP00000477261.1:n.*9+21A>T
NM_000483.4:c.215+21A>T (APOC2)	NP_000474.2:n.215+21A>T
NR_037932.1:n.1422+21A>T (APOC4-APOC2)
NM_000483.5:c.215+21A>T (APOC2) MANE Select	NP_000474.2:n.215+21A>T