Canonical Allele Identifier: CA2493478921

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015178G= , CM000664.2:g.21015178G=	GRCh38
NC_000002.11:g.21238050G= , CM000664.1:g.21238050G=	GRCh37
NC_000002.10:g.21091555G=	NCBI36
NG_011793.1:g.33896C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000673739.2:c.*2897C=	ENSP00000501110.2:n.*2897C=
ENST00000673882.2:c.*2686C=	ENSP00000501253.2:n.*2686C=
ENST00000673739.1:c.3305C=	ENSP00000501110.1:n.3305C=
ENST00000673882.1:c.3094C=	ENSP00000501253.1:n.3094C=
ENST00000233242.5:c.3591C= MANE Select	ENSP00000233242.1:p.Leu1197=
ENST00000616098.4:c.3591C=	ENSP00000477990.1:p.Leu1197=
NM_000384.2:c.3591C=	NP_000375.2:p.Leu1197=
XM_011532809.1:c.3591C=	XP_011531111.1:p.Leu1197=
NM_000384.3:c.3591C= MANE Select	NP_000375.3:p.Leu1197=