Canonical Allele Identifier: CA2261370259

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44385026C= , CM000679.2:g.44385026C=	GRCh38
NC_000017.10:g.42462394C= , CM000679.1:g.42462394C=	GRCh37
NC_000017.9:g.39817920C=	NCBI36
NG_008331.1:g.9480G= , LRG_479:g.9480G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.721G= MANE Select	ENSP00000262407.5:p.Gly241=
ENST00000648408.1:c.152G=
ENST00000262407.5:c.721G=	ENSP00000262407.5:p.Gly241=
ENST00000589645.5:n.172G=
ENST00000591990.5:n.83G=
ENST00000592075.5:n.90G=
ENST00000592226.5:n.39+138G=
ENST00000592253.5:n.229G=
ENST00000592944.1:n.403G=
NM_000419.3:c.721G= , LRG_479t1:c.721G=	NP_000410.2:p.Gly241=
XM_011524749.1:c.721G=	XP_011523051.1:p.Gly241=
XM_011524750.1:c.721G=	XP_011523052.1:p.Gly241=
NM_000419.4:c.721G=	NP_000410.2:p.Gly241=
NM_000419.5:c.721G= MANE Select	NP_000410.2:p.Gly241=