Canonical Allele Identifier: CA2493479009

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015371A= , CM000664.2:g.21015371A=	GRCh38
NC_000002.11:g.21238243A= , CM000664.1:g.21238243A=	GRCh37
NC_000002.10:g.21091748A=	NCBI36
NG_011793.1:g.33703T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2813T=	ENSP00000501110.2:n.*2813T=
ENST00000673882.2:c.*2602T=	ENSP00000501253.2:n.*2602T=
ENST00000673739.1:c.3221T=	ENSP00000501110.1:n.3221T=
ENST00000673882.1:c.3010T=	ENSP00000501253.1:n.3010T=
ENST00000233242.5:c.3507T= MANE Select	ENSP00000233242.1:p.Tyr1169=
ENST00000616098.4:c.3507T=	ENSP00000477990.1:p.Tyr1169=
NM_000384.2:c.3507T=	NP_000375.2:p.Tyr1169=
XM_011532809.1:c.3507T=	XP_011531111.1:p.Tyr1169=
NM_000384.3:c.3507T= MANE Select	NP_000375.3:p.Tyr1169=