Canonical Allele Identifier: CA2493475236

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21007406T= , CM000664.2:g.21007406T=	GRCh38
NC_000002.11:g.21230278T= , CM000664.1:g.21230278T=	GRCh37
NC_000002.10:g.21083783T=	NCBI36
NG_011793.1:g.41668A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233242.5:c.9462A= MANE Select	ENSP00000233242.1:p.Glu3154=
ENST00000616098.4:c.9462A=	ENSP00000477990.1:p.Glu3154=
NM_000384.2:c.9462A=	NP_000375.2:p.Glu3154=
XM_011532809.1:c.5869+3327A=	XP_011531111.1:n.5869+3327A=
NM_000384.3:c.9462A= MANE Select	NP_000375.3:p.Glu3154=