Canonical Allele Identifier: CA2493478918

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015174C= , CM000664.2:g.21015174C=	GRCh38
NC_000002.11:g.21238046C= , CM000664.1:g.21238046C=	GRCh37
NC_000002.10:g.21091551C=	NCBI36
NG_011793.1:g.33900G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000673739.2:c.*2901G=	ENSP00000501110.2:n.*2901G=
ENST00000673882.2:c.*2690G=	ENSP00000501253.2:n.*2690G=
ENST00000673739.1:c.3309G=	ENSP00000501110.1:n.3309G=
ENST00000673882.1:c.3098G=	ENSP00000501253.1:n.3098G=
ENST00000233242.5:c.3595G= MANE Select	ENSP00000233242.1:p.Asp1199=
ENST00000616098.4:c.3595G=	ENSP00000477990.1:p.Asp1199=
NM_000384.2:c.3595G=	NP_000375.2:p.Asp1199=
XM_011532809.1:c.3595G=	XP_011531111.1:p.Asp1199=
NM_000384.3:c.3595G= MANE Select	NP_000375.3:p.Asp1199=