Canonical Allele Identifier: CA406295183

Gene: APOC2 APOC4-APOC2

Linked Data

• MyVariant Identifiers: chr19:g.45452436C>T (hg19) ; chr19:g.44949179C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949179C>T , CM000681.2:g.44949179C>T	GRCh38
NC_000019.9:g.45452436C>T , CM000681.1:g.45452436C>T	GRCh37
NC_000019.8:g.50144276C>T	NCBI36
NG_008837.1:g.8194C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.236C>T (APOC2) MANE Select	ENSP00000252490.5:p.Thr79Ile
ENST00000252490.5:c.236C>T (APOC4-APOC2)	ENSP00000252490.4:p.Thr79Ile
ENST00000585685.5:c.*1019C>T (APOC4-APOC2)	ENSP00000467185.1:n.*1019C>T
ENST00000585786.1:c.*315C>T (APOC2)	ENSP00000465001.1:n.*315C>T
ENST00000589057.5:c.467C>T (APOC4-APOC2)	ENSP00000468139.1:p.Thr156Ile
ENST00000590360.2:c.236C>T (APOC2)	ENSP00000466775.1:p.Thr79Ile
ENST00000591597.5:c.194C>T (APOC2)	ENSP00000476835.1:p.Thr65Ile
ENST00000592257.5:c.*30C>T (APOC2)	ENSP00000477261.1:n.*30C>T
NM_000483.4:c.236C>T (APOC2)	NP_000474.2:p.Thr79Ile
NR_037932.1:n.1443C>T (APOC4-APOC2)
NM_000483.5:c.236C>T (APOC2) MANE Select	NP_000474.2:p.Thr79Ile