Canonical Allele Identifier: CA382711112

Gene: APOC3

Linked Data

• MyVariant Identifiers: chr11:g.116703490A>T (hg19) ; chr11:g.116832774A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116832774A>T , CM000673.2:g.116832774A>T	GRCh38
NC_000011.9:g.116703490A>T , CM000673.1:g.116703490A>T	GRCh37
NC_000011.8:g.116208700A>T	NCBI36
NG_008949.1:g.7867A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000227667.8:c.190A>T MANE Select	ENSP00000227667.2:p.Thr64Ser
ENST00000227667.7:c.190A>T	ENSP00000227667.2:p.Thr64Ser
ENST00000375345.3:c.244A>T	ENSP00000364494.1:p.Thr82Ser
ENST00000630701.1:c.244A>T	ENSP00000486182.1:p.Thr82Ser
NM_000040.1:c.190A>T	NP_000031.1:p.Thr64Ser
NM_000040.2:c.190A>T	NP_000031.1:p.Thr64Ser
NM_000040.3:c.190A>T MANE Select	NP_000031.1:p.Thr64Ser