Canonical Allele Identifier: CA1977847652

Gene: B3GAT3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62616580G= , CM000673.2:g.62616580G=	GRCh38
NC_000011.9:g.62384052G= , CM000673.1:g.62384052G=	GRCh37
NC_000011.8:g.62140628G=	NCBI36
NG_009845.1:g.8840G=
NG_031863.1:g.10596C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265471.10:c.835C= MANE Select	ENSP00000265471.5:p.His279=
ENST00000265471.9:c.835C=	ENSP00000265471.5:p.His279=
ENST00000531383.5:c.835C=	ENSP00000431359.1:p.His279=
ENST00000532585.5:c.*957C=	ENSP00000432604.1:n.*957C=
ENST00000534026.5:c.835C=	ENSP00000432474.1:p.His279=
NM_001288721.1:c.814C=	NP_001275650.1:p.His272=
NM_001288722.1:c.835C=	NP_001275651.1:p.His279=
NM_001288723.1:c.835C=	NP_001275652.1:p.His279=
NM_012200.3:c.835C=	NP_036332.2:p.His279=
NR_109991.1:n.1053C=
XM_011544936.1:c.814C=	XP_011543238.1:p.His272=
NM_012200.4:c.835C= MANE Select	NP_036332.2:p.His279=
NM_001288721.2:c.814C=	NP_001275650.1:p.His272=
NM_001288722.2:c.835C=	NP_001275651.1:p.His279=
NM_001288723.2:c.835C=	NP_001275652.1:p.His279=
NR_109991.2:n.864C=