Canonical Allele Identifier: CA3223275948

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44384113T= , CM000679.2:g.44384113T=	GRCh38
NC_000017.10:g.42461481T= , CM000679.1:g.42461481T=	GRCh37
NC_000017.9:g.39817007T=	NCBI36
NG_008331.1:g.10393A= , LRG_479:g.10393A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000419.5:c.917A= MANE Select	NP_000410.2:p.Gln306=
ENST00000262407.6:c.917A= MANE Select	ENSP00000262407.5:p.Gln306=
NM_000419.3:c.917A= , LRG_479t1:c.917A=	NP_000410.2:p.Gln306=
NM_000419.4:c.917A=	NP_000410.2:p.Gln306=
ENST00000262407.5:c.917A=	ENSP00000262407.5:p.Gln306=
ENST00000589645.5:n.368A=
ENST00000591990.5:n.462A=
ENST00000592075.5:n.286A=
ENST00000592226.5:n.157A=
ENST00000592253.5:n.425A=
ENST00000648408.1:c.348A=
XM_011524749.1:c.917A=	XP_011523051.1:p.Gln306=
XM_011524750.1:c.917A=	XP_011523052.1:p.Gln306=