Canonical Allele Identifier: CA475129319

Gene: B3GAT3

Linked Data

• MyVariant Identifiers: chr11:g.62383999T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62616527T>A , CM000673.2:g.62616527T>A	GRCh38
NC_000011.9:g.62383999T>A , CM000673.1:g.62383999T>A	GRCh37
NC_000011.8:g.62140575T>A	NCBI36
NG_009845.1:g.8787T>A
NG_031863.1:g.10649A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265471.10:c.888A>T MANE Select	ENSP00000265471.5:p.Pro296=
ENST00000265471.9:c.888A>T	ENSP00000265471.5:p.Pro296=
ENST00000531383.5:c.888A>T	ENSP00000431359.1:p.Pro296=
ENST00000532585.5:c.*1010A>T	ENSP00000432604.1:n.*1010A>T
ENST00000534026.5:c.888A>T	ENSP00000432474.1:p.Pro296=
NM_001288721.1:c.867A>T	NP_001275650.1:p.Pro289=
NM_001288722.1:c.888A>T	NP_001275651.1:p.Pro296=
NM_001288723.1:c.888A>T	NP_001275652.1:p.Pro296=
NM_012200.3:c.888A>T	NP_036332.2:p.Pro296=
NR_109991.1:n.1106A>T
XM_011544936.1:c.867A>T	XP_011543238.1:p.Pro289=
NM_012200.4:c.888A>T MANE Select	NP_036332.2:p.Pro296=
NM_001288721.2:c.867A>T	NP_001275650.1:p.Pro289=
NM_001288722.2:c.888A>T	NP_001275651.1:p.Pro296=
NM_001288723.2:c.888A>T	NP_001275652.1:p.Pro296=
NR_109991.2:n.917A>T