Canonical Allele Identifier: CA380974882

Gene: B3GAT3

Linked Data

• MyVariant Identifiers: chr11:g.62383976A>G (hg19) ; chr11:g.62616504A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62616504A>G , CM000673.2:g.62616504A>G	GRCh38
NC_000011.9:g.62383976A>G , CM000673.1:g.62383976A>G	GRCh37
NC_000011.8:g.62140552A>G	NCBI36
NG_009845.1:g.8764A>G
NG_031863.1:g.10672T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265471.10:c.909+2T>C MANE Select	ENSP00000265471.5:n.909+2T>C
ENST00000265471.9:c.909+2T>C	ENSP00000265471.5:n.909+2T>C
ENST00000531383.5:c.909+2T>C	ENSP00000431359.1:n.909+2T>C
ENST00000532585.5:c.*1031+2T>C	ENSP00000432604.1:n.*1031+2T>C
ENST00000534026.5:c.909+2T>C	ENSP00000432474.1:n.909+2T>C
NM_001288721.1:c.888+2T>C	NP_001275650.1:n.888+2T>C
NM_001288722.1:c.909+2T>C	NP_001275651.1:n.909+2T>C
NM_001288723.1:c.909+2T>C	NP_001275652.1:n.909+2T>C
NM_012200.3:c.909+2T>C	NP_036332.2:n.909+2T>C
NR_109991.1:n.1127+2T>C
XM_011544936.1:c.888+2T>C	XP_011543238.1:n.888+2T>C
NM_012200.4:c.909+2T>C MANE Select	NP_036332.2:n.909+2T>C
NM_001288721.2:c.888+2T>C	NP_001275650.1:n.888+2T>C
NM_001288722.2:c.909+2T>C	NP_001275651.1:n.909+2T>C
NM_001288723.2:c.909+2T>C	NP_001275652.1:n.909+2T>C
NR_109991.2:n.938+2T>C