Canonical Allele Identifier: CA380975398

Gene: B3GAT3

Linked Data

• MyVariant Identifiers: chr11:g.62384075A>G (hg19) ; chr11:g.62616603A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62616603A>G , CM000673.2:g.62616603A>G	GRCh38
NC_000011.9:g.62384075A>G , CM000673.1:g.62384075A>G	GRCh37
NC_000011.8:g.62140651A>G	NCBI36
NG_009845.1:g.8863A>G
NG_031863.1:g.10573T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265471.10:c.812T>C MANE Select	ENSP00000265471.5:p.Phe271Ser
ENST00000265471.9:c.812T>C	ENSP00000265471.5:p.Phe271Ser
ENST00000531383.5:c.812T>C	ENSP00000431359.1:p.Phe271Ser
ENST00000532585.5:c.*934T>C	ENSP00000432604.1:n.*934T>C
ENST00000534026.5:c.812T>C	ENSP00000432474.1:p.Phe271Ser
NM_001288721.1:c.791T>C	NP_001275650.1:p.Phe264Ser
NM_001288722.1:c.812T>C	NP_001275651.1:p.Phe271Ser
NM_001288723.1:c.812T>C	NP_001275652.1:p.Phe271Ser
NM_012200.3:c.812T>C	NP_036332.2:p.Phe271Ser
NR_109991.1:n.1030T>C
XM_011544936.1:c.791T>C	XP_011543238.1:p.Phe264Ser
NM_012200.4:c.812T>C MANE Select	NP_036332.2:p.Phe271Ser
NM_001288721.2:c.791T>C	NP_001275650.1:p.Phe264Ser
NM_001288722.2:c.812T>C	NP_001275651.1:p.Phe271Ser
NM_001288723.2:c.812T>C	NP_001275652.1:p.Phe271Ser
NR_109991.2:n.841T>C