Canonical Allele Identifier: CA380975303

Gene: B3GAT3

Linked Data

• dbSNP Id: rs781715246
• gnomAD v4: 11-62616589-G-C
• MyVariant Identifiers: chr11:g.62384061G>C (hg19) ; chr11:g.62616589G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62616589G>C , CM000673.2:g.62616589G>C	GRCh38
NC_000011.9:g.62384061G>C , CM000673.1:g.62384061G>C	GRCh37
NC_000011.8:g.62140637G>C	NCBI36
NG_009845.1:g.8849G>C
NG_031863.1:g.10587C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265471.10:c.826C>G MANE Select	ENSP00000265471.5:p.Pro276Ala
ENST00000265471.9:c.826C>G	ENSP00000265471.5:p.Pro276Ala
ENST00000531383.5:c.826C>G	ENSP00000431359.1:p.Pro276Ala
ENST00000532585.5:c.*948C>G	ENSP00000432604.1:n.*948C>G
ENST00000534026.5:c.826C>G	ENSP00000432474.1:p.Pro276Ala
NM_001288721.1:c.805C>G	NP_001275650.1:p.Pro269Ala
NM_001288722.1:c.826C>G	NP_001275651.1:p.Pro276Ala
NM_001288723.1:c.826C>G	NP_001275652.1:p.Pro276Ala
NM_012200.3:c.826C>G	NP_036332.2:p.Pro276Ala
NR_109991.1:n.1044C>G
XM_011544936.1:c.805C>G	XP_011543238.1:p.Pro269Ala
NM_012200.4:c.826C>G MANE Select	NP_036332.2:p.Pro276Ala
NM_001288721.2:c.805C>G	NP_001275650.1:p.Pro269Ala
NM_001288722.2:c.826C>G	NP_001275651.1:p.Pro276Ala
NM_001288723.2:c.826C>G	NP_001275652.1:p.Pro276Ala
NR_109991.2:n.855C>G