Canonical Allele Identifier: CA2493474278

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21005166C= , CM000664.2:g.21005166C=	GRCh38
NC_000002.11:g.21228038C= , CM000664.1:g.21228038C=	GRCh37
NC_000002.10:g.21081543C=	NCBI36
NG_011793.1:g.43908G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000233242.5:c.11702G= MANE Select	ENSP00000233242.1:p.Ser3901=
ENST00000616098.4:c.11702G=	ENSP00000477990.1:p.Ser3901=
NM_000384.2:c.11702G=	NP_000375.2:p.Ser3901=
XM_011532809.1:c.5869+5567G=	XP_011531111.1:n.5869+5567G=
NM_000384.3:c.11702G= MANE Select	NP_000375.3:p.Ser3901=