Canonical Allele Identifier: CA380975418

Gene: B3GAT3

Linked Data

• MyVariant Identifiers: chr11:g.62384078T>C (hg19) ; chr11:g.62616606T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62616606T>C , CM000673.2:g.62616606T>C	GRCh38
NC_000011.9:g.62384078T>C , CM000673.1:g.62384078T>C	GRCh37
NC_000011.8:g.62140654T>C	NCBI36
NG_009845.1:g.8866T>C
NG_031863.1:g.10570A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265471.10:c.809A>G MANE Select	ENSP00000265471.5:p.Gln270Arg
ENST00000265471.9:c.809A>G	ENSP00000265471.5:p.Gln270Arg
ENST00000531383.5:c.809A>G	ENSP00000431359.1:p.Gln270Arg
ENST00000532585.5:c.*931A>G	ENSP00000432604.1:n.*931A>G
ENST00000534026.5:c.809A>G	ENSP00000432474.1:p.Gln270Arg
NM_001288721.1:c.788A>G	NP_001275650.1:p.Gln263Arg
NM_001288722.1:c.809A>G	NP_001275651.1:p.Gln270Arg
NM_001288723.1:c.809A>G	NP_001275652.1:p.Gln270Arg
NM_012200.3:c.809A>G	NP_036332.2:p.Gln270Arg
NR_109991.1:n.1027A>G
XM_011544936.1:c.788A>G	XP_011543238.1:p.Gln263Arg
NM_012200.4:c.809A>G MANE Select	NP_036332.2:p.Gln270Arg
NM_001288721.2:c.788A>G	NP_001275650.1:p.Gln263Arg
NM_001288722.2:c.809A>G	NP_001275651.1:p.Gln270Arg
NM_001288723.2:c.809A>G	NP_001275652.1:p.Gln270Arg
NR_109991.2:n.838A>G