Canonical Allele Identifier: CA2493478917

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015173T= , CM000664.2:g.21015173T=	GRCh38
NC_000002.11:g.21238045T= , CM000664.1:g.21238045T=	GRCh37
NC_000002.10:g.21091550T=	NCBI36
NG_011793.1:g.33901A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000673739.2:c.*2902A=	ENSP00000501110.2:n.*2902A=
ENST00000673882.2:c.*2691A=	ENSP00000501253.2:n.*2691A=
ENST00000673739.1:c.3310A=	ENSP00000501110.1:n.3310A=
ENST00000673882.1:c.3099A=	ENSP00000501253.1:n.3099A=
ENST00000233242.5:c.3596A= MANE Select	ENSP00000233242.1:p.Asp1199=
ENST00000616098.4:c.3596A=	ENSP00000477990.1:p.Asp1199=
NM_000384.2:c.3596A=	NP_000375.2:p.Asp1199=
XM_011532809.1:c.3596A=	XP_011531111.1:p.Asp1199=
NM_000384.3:c.3596A= MANE Select	NP_000375.3:p.Asp1199=