Canonical Allele Identifier: CA2261370015

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44384570A= , CM000679.2:g.44384570A=	GRCh38
NC_000017.10:g.42461938A= , CM000679.1:g.42461938A=	GRCh37
NC_000017.9:g.39817464A=	NCBI36
NG_008331.1:g.9936T= , LRG_479:g.9936T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.815T= MANE Select	ENSP00000262407.5:p.Val272=
ENST00000648408.1:c.246T=
ENST00000262407.5:c.815T=	ENSP00000262407.5:p.Val272=
ENST00000589645.5:n.266T=
ENST00000591990.5:n.177T=
ENST00000592075.5:n.184T=
ENST00000592226.5:n.55T=
ENST00000592253.5:n.323T=
ENST00000592944.1:n.497T=
NM_000419.3:c.815T= , LRG_479t1:c.815T=	NP_000410.2:p.Val272=
XM_011524749.1:c.815T=	XP_011523051.1:p.Val272=
XM_011524750.1:c.815T=	XP_011523052.1:p.Val272=
NM_000419.4:c.815T=	NP_000410.2:p.Val272=
NM_000419.5:c.815T= MANE Select	NP_000410.2:p.Val272=