Canonical Allele Identifier: CA2493475327

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21007571G= , CM000664.2:g.21007571G=	GRCh38
NC_000002.11:g.21230443G= , CM000664.1:g.21230443G=	GRCh37
NC_000002.10:g.21083948G=	NCBI36
NG_011793.1:g.41503C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000233242.5:c.9297C= MANE Select	ENSP00000233242.1:p.Asn3099=
ENST00000616098.4:c.9297C=	ENSP00000477990.1:p.Asn3099=
NM_000384.2:c.9297C=	NP_000375.2:p.Asn3099=
XM_011532809.1:c.5869+3162C=	XP_011531111.1:n.5869+3162C=
NM_000384.3:c.9297C= MANE Select	NP_000375.3:p.Asn3099=