Canonical Allele Identifier: CA2493478075

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21013289A= , CM000664.2:g.21013289A=	GRCh38
NC_000002.11:g.21236161A= , CM000664.1:g.21236161A=	GRCh37
NC_000002.10:g.21089666A=	NCBI36
NG_011793.1:g.35785T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000673739.2:c.*3393T=	ENSP00000501110.2:n.*3393T=
ENST00000673739.1:c.3801T=	ENSP00000501110.1:n.3801T=
ENST00000233242.5:c.4087T= MANE Select	ENSP00000233242.1:p.Tyr1363=
ENST00000616098.4:c.4087T=	ENSP00000477990.1:p.Tyr1363=
NM_000384.2:c.4087T=	NP_000375.2:p.Tyr1363=
XM_011532809.1:c.4087T=	XP_011531111.1:p.Tyr1363=
NM_000384.3:c.4087T= MANE Select	NP_000375.3:p.Tyr1363=