Canonical Allele Identifier: CA2493479050

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015467G= , CM000664.2:g.21015467G=	GRCh38
NC_000002.11:g.21238339G= , CM000664.1:g.21238339G=	GRCh37
NC_000002.10:g.21091844G=	NCBI36
NG_011793.1:g.33607C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2717C=	ENSP00000501110.2:n.*2717C=
ENST00000673882.2:c.*2506C=	ENSP00000501253.2:n.*2506C=
ENST00000673739.1:c.3125C=	ENSP00000501110.1:n.3125C=
ENST00000673882.1:c.2914C=	ENSP00000501253.1:n.2914C=
ENST00000233242.5:c.3411C= MANE Select	ENSP00000233242.1:p.Ile1137=
ENST00000616098.4:c.3411C=	ENSP00000477990.1:p.Ile1137=
NM_000384.2:c.3411C=	NP_000375.2:p.Ile1137=
XM_011532809.1:c.3411C=	XP_011531111.1:p.Ile1137=
NM_000384.3:c.3411C= MANE Select	NP_000375.3:p.Ile1137=