Canonical Allele Identifier: CA2493478943

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015221T= , CM000664.2:g.21015221T=	GRCh38
NC_000002.11:g.21238093T= , CM000664.1:g.21238093T=	GRCh37
NC_000002.10:g.21091598T=	NCBI36
NG_011793.1:g.33853A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2854A=	ENSP00000501110.2:n.*2854A=
ENST00000673882.2:c.*2643A=	ENSP00000501253.2:n.*2643A=
ENST00000673739.1:c.3262A=	ENSP00000501110.1:n.3262A=
ENST00000673882.1:c.3051A=	ENSP00000501253.1:n.3051A=
ENST00000233242.5:c.3548A= MANE Select	ENSP00000233242.1:p.Asn1183=
ENST00000616098.4:c.3548A=	ENSP00000477990.1:p.Asn1183=
NM_000384.2:c.3548A=	NP_000375.2:p.Asn1183=
XM_011532809.1:c.3548A=	XP_011531111.1:p.Asn1183=
NM_000384.3:c.3548A= MANE Select	NP_000375.3:p.Asn1183=