Canonical Allele Identifier: CA2493488928

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21037162G= , CM000664.2:g.21037162G=	GRCh38
NC_000002.11:g.21260034G= , CM000664.1:g.21260034G=	GRCh37
NC_000002.10:g.21113539G=	NCBI36
NG_011793.1:g.11912C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.477C=	ENSP00000501110.2:p.Gly159=
ENST00000673882.2:c.477C=	ENSP00000501253.2:p.Gly159=
ENST00000673739.1:c.345C=	ENSP00000501110.1:p.Gly115=
ENST00000673882.1:c.345C=	ENSP00000501253.1:p.Gly115=
ENST00000233242.5:c.631C= MANE Select	ENSP00000233242.1:p.Gln211=
ENST00000399256.4:c.631C=	ENSP00000382200.4:p.Gln211=
ENST00000616098.4:c.631C=	ENSP00000477990.1:p.Gln211=
NM_000384.2:c.631C=	NP_000375.2:p.Gln211=
XM_011532809.1:c.631C=	XP_011531111.1:p.Gln211=
NM_000384.3:c.631C= MANE Select	NP_000375.3:p.Gln211=