Canonical Allele Identifier: CA2493475332

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21007581T= , CM000664.2:g.21007581T=	GRCh38
NC_000002.11:g.21230453T= , CM000664.1:g.21230453T=	GRCh37
NC_000002.10:g.21083958T=	NCBI36
NG_011793.1:g.41493A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000233242.5:c.9287A= MANE Select	ENSP00000233242.1:p.Tyr3096=
ENST00000616098.4:c.9287A=	ENSP00000477990.1:p.Tyr3096=
NM_000384.2:c.9287A=	NP_000375.2:p.Tyr3096=
XM_011532809.1:c.5869+3152A=	XP_011531111.1:n.5869+3152A=
NM_000384.3:c.9287A= MANE Select	NP_000375.3:p.Tyr3096=