Canonical Allele Identifier: CA2493479055

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015491C= , CM000664.2:g.21015491C=	GRCh38
NC_000002.11:g.21238363C= , CM000664.1:g.21238363C=	GRCh37
NC_000002.10:g.21091868C=	NCBI36
NG_011793.1:g.33583G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2693G=	ENSP00000501110.2:n.*2693G=
ENST00000673882.2:c.*2482G=	ENSP00000501253.2:n.*2482G=
ENST00000673739.1:c.3101G=	ENSP00000501110.1:n.3101G=
ENST00000673882.1:c.2890G=	ENSP00000501253.1:n.2890G=
ENST00000233242.5:c.3387G= MANE Select	ENSP00000233242.1:p.Leu1129=
ENST00000616098.4:c.3387G=	ENSP00000477990.1:p.Leu1129=
NM_000384.2:c.3387G=	NP_000375.2:p.Leu1129=
XM_011532809.1:c.3387G=	XP_011531111.1:p.Leu1129=
NM_000384.3:c.3387G= MANE Select	NP_000375.3:p.Leu1129=