Canonical Allele Identifier: CA1977848146

Gene: B3GAT3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62616748C= , CM000673.2:g.62616748C=	GRCh38
NC_000011.9:g.62384220C= , CM000673.1:g.62384220C=	GRCh37
NC_000011.8:g.62140796C=	NCBI36
NG_009845.1:g.9008C=
NG_031863.1:g.10428G=

Transcript Alleles

HGVS	Amino-acid Change
NM_012200.4:c.667G= MANE Select	NP_036332.2:p.Gly223=
ENST00000265471.10:c.667G= MANE Select	ENSP00000265471.5:p.Gly223=
NM_001288721.1:c.646G=	NP_001275650.1:p.Gly216=
NM_001288721.2:c.646G=	NP_001275650.1:p.Gly216=
NM_001288722.1:c.667G=	NP_001275651.1:p.Gly223=
NM_001288722.2:c.667G=	NP_001275651.1:p.Gly223=
NM_001288723.1:c.667G=	NP_001275652.1:p.Gly223=
NM_001288723.2:c.667G=	NP_001275652.1:p.Gly223=
NM_012200.3:c.667G=	NP_036332.2:p.Gly223=
NR_109991.1:n.885G=
NR_109991.2:n.696G=
ENST00000265471.9:c.667G=	ENSP00000265471.5:p.Gly223=
ENST00000531383.5:c.667G=	ENSP00000431359.1:p.Gly223=
ENST00000532585.5:c.*789G=	ENSP00000432604.1:n.*789G=
ENST00000533303.1:n.517G=
ENST00000534026.5:c.667G=	ENSP00000432474.1:p.Gly223=
XM_011544936.1:c.646G=	XP_011543238.1:p.Gly216=