Canonical Allele Identifier: CA1977847990

Gene: B3GAT3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62616706C= , CM000673.2:g.62616706C=	GRCh38
NC_000011.9:g.62384178C= , CM000673.1:g.62384178C=	GRCh37
NC_000011.8:g.62140754C=	NCBI36
NG_009845.1:g.8966C=
NG_031863.1:g.10470G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265471.10:c.709G= MANE Select	ENSP00000265471.5:p.Val237=
ENST00000265471.9:c.709G=	ENSP00000265471.5:p.Val237=
ENST00000531383.5:c.709G=	ENSP00000431359.1:p.Val237=
ENST00000532585.5:c.*831G=	ENSP00000432604.1:n.*831G=
ENST00000533303.1:n.559G=
ENST00000534026.5:c.709G=	ENSP00000432474.1:p.Val237=
NM_001288721.1:c.688G=	NP_001275650.1:p.Val230=
NM_001288722.1:c.709G=	NP_001275651.1:p.Val237=
NM_001288723.1:c.709G=	NP_001275652.1:p.Val237=
NM_012200.3:c.709G=	NP_036332.2:p.Val237=
NR_109991.1:n.927G=
XM_011544936.1:c.688G=	XP_011543238.1:p.Val230=
NM_012200.4:c.709G= MANE Select	NP_036332.2:p.Val237=
NM_001288721.2:c.688G=	NP_001275650.1:p.Val230=
NM_001288722.2:c.709G=	NP_001275651.1:p.Val237=
NM_001288723.2:c.709G=	NP_001275652.1:p.Val237=
NR_109991.2:n.738G=