Canonical Allele Identifier: CA1977847670

Gene: B3GAT3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62616589G= , CM000673.2:g.62616589G=	GRCh38
NC_000011.9:g.62384061G= , CM000673.1:g.62384061G=	GRCh37
NC_000011.8:g.62140637G=	NCBI36
NG_009845.1:g.8849G=
NG_031863.1:g.10587C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265471.10:c.826C= MANE Select	ENSP00000265471.5:p.Pro276=
ENST00000265471.9:c.826C=	ENSP00000265471.5:p.Pro276=
ENST00000531383.5:c.826C=	ENSP00000431359.1:p.Pro276=
ENST00000532585.5:c.*948C=	ENSP00000432604.1:n.*948C=
ENST00000534026.5:c.826C=	ENSP00000432474.1:p.Pro276=
NM_001288721.1:c.805C=	NP_001275650.1:p.Pro269=
NM_001288722.1:c.826C=	NP_001275651.1:p.Pro276=
NM_001288723.1:c.826C=	NP_001275652.1:p.Pro276=
NM_012200.3:c.826C=	NP_036332.2:p.Pro276=
NR_109991.1:n.1044C=
XM_011544936.1:c.805C=	XP_011543238.1:p.Pro269=
NM_012200.4:c.826C= MANE Select	NP_036332.2:p.Pro276=
NM_001288721.2:c.805C=	NP_001275650.1:p.Pro269=
NM_001288722.2:c.826C=	NP_001275651.1:p.Pro276=
NM_001288723.2:c.826C=	NP_001275652.1:p.Pro276=
NR_109991.2:n.855C=