Canonical Allele Identifier: CA2725023798

Gene: APOC3

Linked Data

• dbSNP Id: rs2134224759

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116830768C>T , CM000673.2:g.116830768C>T	GRCh38
NC_000011.9:g.116701484C>T , CM000673.1:g.116701484C>T	GRCh37
NC_000011.8:g.116206694C>T	NCBI36
NG_008949.1:g.5861C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000227667.8:c.56-5C>T MANE Select	ENSP00000227667.2:n.56-5C>T
ENST00000227667.7:c.56-5C>T	ENSP00000227667.2:n.56-5C>T
ENST00000375345.3:c.110-5C>T	ENSP00000364494.1:n.110-5C>T
ENST00000433777.5:c.56-5C>T	ENSP00000410614.1:n.56-5C>T
ENST00000470144.1:n.88-5C>T
ENST00000630701.1:c.110-5C>T	ENSP00000486182.1:n.110-5C>T
NM_000040.1:c.56-5C>T	NP_000031.1:n.56-5C>T
NM_000040.2:c.56-5C>T	NP_000031.1:n.56-5C>T
NM_000040.3:c.56-5C>T MANE Select	NP_000031.1:n.56-5C>T