Canonical Allele Identifier: CA2261365251

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374449C= , CM000679.2:g.44374449C=	GRCh38
NC_000017.10:g.42451817C= , CM000679.1:g.42451817C=	GRCh37
NC_000017.9:g.39807343C=	NCBI36
NG_008331.1:g.20057G= , LRG_479:g.20057G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000419.5:c.2965G= MANE Select	NP_000410.2:p.Ala989=
ENST00000262407.6:c.2965G= MANE Select	ENSP00000262407.5:p.Ala989=
NM_000419.3:c.2965G= , LRG_479t1:c.2965G=	NP_000410.2:p.Ala989=
NM_000419.4:c.2965G=	NP_000410.2:p.Ala989=
ENST00000262407.5:c.2965G=	ENSP00000262407.5:p.Ala989=
ENST00000587295.5:c.253+1384G=
ENST00000588098.1:c.37+210G=
ENST00000592462.5:n.2664G=
ENST00000648408.1:c.2374+210G=
XM_011524749.1:c.2863G=	XP_011523051.1:p.Ala955=
XM_011524750.1:c.2943+210G=	XP_011523052.1:n.2943+210G=