Canonical Allele Identifier: CA2493478920

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015177A= , CM000664.2:g.21015177A=	GRCh38
NC_000002.11:g.21238049A= , CM000664.1:g.21238049A=	GRCh37
NC_000002.10:g.21091554A=	NCBI36
NG_011793.1:g.33897T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000673739.2:c.*2898T=	ENSP00000501110.2:n.*2898T=
ENST00000673882.2:c.*2687T=	ENSP00000501253.2:n.*2687T=
ENST00000673739.1:c.3306T=	ENSP00000501110.1:n.3306T=
ENST00000673882.1:c.3095T=	ENSP00000501253.1:n.3095T=
ENST00000233242.5:c.3592T= MANE Select	ENSP00000233242.1:p.Ser1198=
ENST00000616098.4:c.3592T=	ENSP00000477990.1:p.Ser1198=
NM_000384.2:c.3592T=	NP_000375.2:p.Ser1198=
XM_011532809.1:c.3592T=	XP_011531111.1:p.Ser1198=
NM_000384.3:c.3592T= MANE Select	NP_000375.3:p.Ser1198=