Canonical Allele Identifier: CA2002758766

Gene: APOC3

Linked Data

• dbSNP Id: rs1404007727

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116830549T>C , CM000673.2:g.116830549T>C	GRCh38
NC_000011.9:g.116701265T>C , CM000673.1:g.116701265T>C	GRCh37
NC_000011.8:g.116206475T>C	NCBI36
NG_008949.1:g.5642T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227667.8:c.-13-21T>C MANE Select	ENSP00000227667.2:n.-13-21T>C
ENST00000227667.7:c.-13-21T>C	ENSP00000227667.2:n.-13-21T>C
ENST00000375345.3:c.21T>C	ENSP00000364494.1:p.Pro7=
ENST00000433777.5:c.-13-21T>C	ENSP00000410614.1:n.-13-21T>C
ENST00000470144.1:n.20-21T>C
ENST00000630701.1:c.21T>C	ENSP00000486182.1:p.Pro7=
NM_000040.1:c.-13-21T>C	NP_000031.1:n.-13-21T>C
NM_000040.2:c.-13-21T>C	NP_000031.1:n.-13-21T>C
NM_000040.3:c.-13-21T>C MANE Select	NP_000031.1:n.-13-21T>C