Canonical Allele Identifier: CA2493479048

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015465A= , CM000664.2:g.21015465A=	GRCh38
NC_000002.11:g.21238337A= , CM000664.1:g.21238337A=	GRCh37
NC_000002.10:g.21091842A=	NCBI36
NG_011793.1:g.33609T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2719T=	ENSP00000501110.2:n.*2719T=
ENST00000673882.2:c.*2508T=	ENSP00000501253.2:n.*2508T=
ENST00000673739.1:c.3127T=	ENSP00000501110.1:n.3127T=
ENST00000673882.1:c.2916T=	ENSP00000501253.1:n.2916T=
ENST00000233242.5:c.3413T= MANE Select	ENSP00000233242.1:p.Leu1138=
ENST00000616098.4:c.3413T=	ENSP00000477990.1:p.Leu1138=
NM_000384.2:c.3413T=	NP_000375.2:p.Leu1138=
XM_011532809.1:c.3413T=	XP_011531111.1:p.Leu1138=
NM_000384.3:c.3413T= MANE Select	NP_000375.3:p.Leu1138=