Canonical Allele Identifier: CA1977847659

Gene: B3GAT3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62616585C= , CM000673.2:g.62616585C=	GRCh38
NC_000011.9:g.62384057C= , CM000673.1:g.62384057C=	GRCh37
NC_000011.8:g.62140633C=	NCBI36
NG_009845.1:g.8845C=
NG_031863.1:g.10591G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265471.10:c.830G= MANE Select	ENSP00000265471.5:p.Arg277=
ENST00000265471.9:c.830G=	ENSP00000265471.5:p.Arg277=
ENST00000531383.5:c.830G=	ENSP00000431359.1:p.Arg277=
ENST00000532585.5:c.*952G=	ENSP00000432604.1:n.*952G=
ENST00000534026.5:c.830G=	ENSP00000432474.1:p.Arg277=
NM_001288721.1:c.809G=	NP_001275650.1:p.Arg270=
NM_001288722.1:c.830G=	NP_001275651.1:p.Arg277=
NM_001288723.1:c.830G=	NP_001275652.1:p.Arg277=
NM_012200.3:c.830G=	NP_036332.2:p.Arg277=
NR_109991.1:n.1048G=
XM_011544936.1:c.809G=	XP_011543238.1:p.Arg270=
NM_012200.4:c.830G= MANE Select	NP_036332.2:p.Arg277=
NM_001288721.2:c.809G=	NP_001275650.1:p.Arg270=
NM_001288722.2:c.830G=	NP_001275651.1:p.Arg277=
NM_001288723.2:c.830G=	NP_001275652.1:p.Arg277=
NR_109991.2:n.859G=