Canonical Allele Identifier: CA475129281

Gene: B3GAT3

Linked Data

• MyVariant Identifiers: chr11:g.62383981A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62616509A>G , CM000673.2:g.62616509A>G	GRCh38
NC_000011.9:g.62383981A>G , CM000673.1:g.62383981A>G	GRCh37
NC_000011.8:g.62140557A>G	NCBI36
NG_009845.1:g.8769A>G
NG_031863.1:g.10667T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265471.10:c.906T>C MANE Select	ENSP00000265471.5:p.Thr302=
ENST00000265471.9:c.906T>C	ENSP00000265471.5:p.Thr302=
ENST00000531383.5:c.906T>C	ENSP00000431359.1:p.Thr302=
ENST00000532585.5:c.*1028T>C	ENSP00000432604.1:n.*1028T>C
ENST00000534026.5:c.906T>C	ENSP00000432474.1:p.Thr302=
NM_001288721.1:c.885T>C	NP_001275650.1:p.Thr295=
NM_001288722.1:c.906T>C	NP_001275651.1:p.Thr302=
NM_001288723.1:c.906T>C	NP_001275652.1:p.Thr302=
NM_012200.3:c.906T>C	NP_036332.2:p.Thr302=
NR_109991.1:n.1124T>C
XM_011544936.1:c.885T>C	XP_011543238.1:p.Thr295=
NM_012200.4:c.906T>C MANE Select	NP_036332.2:p.Thr302=
NM_001288721.2:c.885T>C	NP_001275650.1:p.Thr295=
NM_001288722.2:c.906T>C	NP_001275651.1:p.Thr302=
NM_001288723.2:c.906T>C	NP_001275652.1:p.Thr302=
NR_109991.2:n.935T>C