Canonical Allele Identifier: CA2261370017

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44384572G= , CM000679.2:g.44384572G=	GRCh38
NC_000017.10:g.42461940G= , CM000679.1:g.42461940G=	GRCh37
NC_000017.9:g.39817466G=	NCBI36
NG_008331.1:g.9934C= , LRG_479:g.9934C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.813C= MANE Select	ENSP00000262407.5:p.Ala271=
ENST00000648408.1:c.244C=
ENST00000262407.5:c.813C=	ENSP00000262407.5:p.Ala271=
ENST00000589645.5:n.264C=
ENST00000591990.5:n.175C=
ENST00000592075.5:n.182C=
ENST00000592226.5:n.53C=
ENST00000592253.5:n.321C=
ENST00000592944.1:n.495C=
NM_000419.3:c.813C= , LRG_479t1:c.813C=	NP_000410.2:p.Ala271=
XM_011524749.1:c.813C=	XP_011523051.1:p.Ala271=
XM_011524750.1:c.813C=	XP_011523052.1:p.Ala271=
NM_000419.4:c.813C=	NP_000410.2:p.Ala271=
NM_000419.5:c.813C= MANE Select	NP_000410.2:p.Ala271=