Canonical Allele Identifier: CA2493478074

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21013288T= , CM000664.2:g.21013288T=	GRCh38
NC_000002.11:g.21236160T= , CM000664.1:g.21236160T=	GRCh37
NC_000002.10:g.21089665T=	NCBI36
NG_011793.1:g.35786A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*3394A=	ENSP00000501110.2:n.*3394A=
ENST00000673739.1:c.3802A=	ENSP00000501110.1:n.3802A=
ENST00000233242.5:c.4088A= MANE Select	ENSP00000233242.1:p.Tyr1363=
ENST00000616098.4:c.4088A=	ENSP00000477990.1:p.Tyr1363=
NM_000384.2:c.4088A=	NP_000375.2:p.Tyr1363=
XM_011532809.1:c.4088A=	XP_011531111.1:p.Tyr1363=
NM_000384.3:c.4088A= MANE Select	NP_000375.3:p.Tyr1363=