Canonical Allele Identifier: CA2493474238

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21005076T= , CM000664.2:g.21005076T=	GRCh38
NC_000002.11:g.21227948T= , CM000664.1:g.21227948T=	GRCh37
NC_000002.10:g.21081453T=	NCBI36
NG_011793.1:g.43998A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000233242.5:c.11788+4A= MANE Select	ENSP00000233242.1:n.11788+4A=
ENST00000616098.4:c.11788+4A=	ENSP00000477990.1:n.11788+4A=
NM_000384.2:c.11788+4A=	NP_000375.2:n.11788+4A=
XM_011532809.1:c.5869+5657A=	XP_011531111.1:n.5869+5657A=
NM_000384.3:c.11788+4A= MANE Select	NP_000375.3:n.11788+4A=