Canonical Allele Identifier: CA380975404

Gene: B3GAT3

Linked Data

• MyVariant Identifiers: chr11:g.62384076A>C (hg19) ; chr11:g.62616604A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62616604A>C , CM000673.2:g.62616604A>C	GRCh38
NC_000011.9:g.62384076A>C , CM000673.1:g.62384076A>C	GRCh37
NC_000011.8:g.62140652A>C	NCBI36
NG_009845.1:g.8864A>C
NG_031863.1:g.10572T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265471.10:c.811T>G MANE Select	ENSP00000265471.5:p.Phe271Val
ENST00000265471.9:c.811T>G	ENSP00000265471.5:p.Phe271Val
ENST00000531383.5:c.811T>G	ENSP00000431359.1:p.Phe271Val
ENST00000532585.5:c.*933T>G	ENSP00000432604.1:n.*933T>G
ENST00000534026.5:c.811T>G	ENSP00000432474.1:p.Phe271Val
NM_001288721.1:c.790T>G	NP_001275650.1:p.Phe264Val
NM_001288722.1:c.811T>G	NP_001275651.1:p.Phe271Val
NM_001288723.1:c.811T>G	NP_001275652.1:p.Phe271Val
NM_012200.3:c.811T>G	NP_036332.2:p.Phe271Val
NR_109991.1:n.1029T>G
XM_011544936.1:c.790T>G	XP_011543238.1:p.Phe264Val
NM_012200.4:c.811T>G MANE Select	NP_036332.2:p.Phe271Val
NM_001288721.2:c.790T>G	NP_001275650.1:p.Phe264Val
NM_001288722.2:c.811T>G	NP_001275651.1:p.Phe271Val
NM_001288723.2:c.811T>G	NP_001275652.1:p.Phe271Val
NR_109991.2:n.840T>G