Canonical Allele Identifier: CA2493478942

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015220A= , CM000664.2:g.21015220A=	GRCh38
NC_000002.11:g.21238092A= , CM000664.1:g.21238092A=	GRCh37
NC_000002.10:g.21091597A=	NCBI36
NG_011793.1:g.33854T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2855T=	ENSP00000501110.2:n.*2855T=
ENST00000673882.2:c.*2644T=	ENSP00000501253.2:n.*2644T=
ENST00000673739.1:c.3263T=	ENSP00000501110.1:n.3263T=
ENST00000673882.1:c.3052T=	ENSP00000501253.1:n.3052T=
ENST00000233242.5:c.3549T= MANE Select	ENSP00000233242.1:p.Asn1183=
ENST00000616098.4:c.3549T=	ENSP00000477990.1:p.Asn1183=
NM_000384.2:c.3549T=	NP_000375.2:p.Asn1183=
XM_011532809.1:c.3549T=	XP_011531111.1:p.Asn1183=
NM_000384.3:c.3549T= MANE Select	NP_000375.3:p.Asn1183=