Canonical Allele Identifier: CA475129512

Gene: B3GAT3

Linked Data

• MyVariant Identifiers: chr11:g.62384059G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62616587G>C , CM000673.2:g.62616587G>C	GRCh38
NC_000011.9:g.62384059G>C , CM000673.1:g.62384059G>C	GRCh37
NC_000011.8:g.62140635G>C	NCBI36
NG_009845.1:g.8847G>C
NG_031863.1:g.10589C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265471.10:c.828C>G MANE Select	ENSP00000265471.5:p.Pro276=
ENST00000265471.9:c.828C>G	ENSP00000265471.5:p.Pro276=
ENST00000531383.5:c.828C>G	ENSP00000431359.1:p.Pro276=
ENST00000532585.5:c.*950C>G	ENSP00000432604.1:n.*950C>G
ENST00000534026.5:c.828C>G	ENSP00000432474.1:p.Pro276=
NM_001288721.1:c.807C>G	NP_001275650.1:p.Pro269=
NM_001288722.1:c.828C>G	NP_001275651.1:p.Pro276=
NM_001288723.1:c.828C>G	NP_001275652.1:p.Pro276=
NM_012200.3:c.828C>G	NP_036332.2:p.Pro276=
NR_109991.1:n.1046C>G
XM_011544936.1:c.807C>G	XP_011543238.1:p.Pro269=
NM_012200.4:c.828C>G MANE Select	NP_036332.2:p.Pro276=
NM_001288721.2:c.807C>G	NP_001275650.1:p.Pro269=
NM_001288722.2:c.828C>G	NP_001275651.1:p.Pro276=
NM_001288723.2:c.828C>G	NP_001275652.1:p.Pro276=
NR_109991.2:n.857C>G