Canonical Allele Identifier: CA2493474990

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21006824G= , CM000664.2:g.21006824G=	GRCh38
NC_000002.11:g.21229696G= , CM000664.1:g.21229696G=	GRCh37
NC_000002.10:g.21083201G=	NCBI36
NG_011793.1:g.42250C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233242.5:c.10044C= MANE Select	ENSP00000233242.1:p.Ile3348=
ENST00000616098.4:c.10044C=	ENSP00000477990.1:p.Ile3348=
NM_000384.2:c.10044C=	NP_000375.2:p.Ile3348=
XM_011532809.1:c.5869+3909C=	XP_011531111.1:n.5869+3909C=
NM_000384.3:c.10044C= MANE Select	NP_000375.3:p.Ile3348=