Canonical Allele Identifier: CA2493484918

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21028358T= , CM000664.2:g.21028358T=	GRCh38
NC_000002.11:g.21251230T= , CM000664.1:g.21251230T=	GRCh37
NC_000002.10:g.21104735T=	NCBI36
NG_011793.1:g.20716A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*1104A=	ENSP00000501110.2:n.*1104A=
ENST00000673882.2:c.*1104A=	ENSP00000501253.2:n.*1104A=
ENST00000673739.1:c.1512A=	ENSP00000501110.1:n.1512A=
ENST00000673882.1:c.1512A=	ENSP00000501253.1:n.1512A=
ENST00000233242.5:c.1798A= MANE Select	ENSP00000233242.1:p.Ile600=
ENST00000399256.4:c.1798A=	ENSP00000382200.4:p.Ile600=
ENST00000616098.4:c.1798A=	ENSP00000477990.1:p.Ile600=
NM_000384.2:c.1798A=	NP_000375.2:p.Ile600=
XM_011532809.1:c.1798A=	XP_011531111.1:p.Ile600=
NM_000384.3:c.1798A= MANE Select	NP_000375.3:p.Ile600=