Canonical Allele Identifier: CA2493489273

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21037962A= , CM000664.2:g.21037962A=	GRCh38
NC_000002.11:g.21260834A= , CM000664.1:g.21260834A=	GRCh37
NC_000002.10:g.21114339A=	NCBI36
NG_011793.1:g.11112T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000673739.2:c.384-707T=	ENSP00000501110.2:n.384-707T=
ENST00000673882.2:c.384-707T=	ENSP00000501253.2:n.384-707T=
ENST00000673739.1:c.252-707T=	ENSP00000501110.1:n.252-707T=
ENST00000673882.1:c.252-707T=	ENSP00000501253.1:n.252-707T=
ENST00000233242.5:c.533T= MANE Select	ENSP00000233242.1:p.Phe178=
ENST00000399256.4:c.533T=	ENSP00000382200.4:p.Phe178=
ENST00000616098.4:c.533T=	ENSP00000477990.1:p.Phe178=
NM_000384.2:c.533T=	NP_000375.2:p.Phe178=
XM_011532809.1:c.533T=	XP_011531111.1:p.Phe178=
NM_000384.3:c.533T= MANE Select	NP_000375.3:p.Phe178=