Canonical Allele Identifier: CA2261365200

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374352A= , CM000679.2:g.44374352A=	GRCh38
NC_000017.10:g.42451720A= , CM000679.1:g.42451720A=	GRCh37
NC_000017.9:g.39807246A=	NCBI36
NG_008331.1:g.20154T= , LRG_479:g.20154T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000419.5:c.3060+2T= MANE Select	NP_000410.2:n.3060+2T=
ENST00000262407.6:c.3060+2T= MANE Select	ENSP00000262407.5:n.3060+2T=
NM_000419.3:c.3060+2T= , LRG_479t1:c.3060+2T=	NP_000410.2:n.3060+2T=
NM_000419.4:c.3060+2T=	NP_000410.2:n.3060+2T=
ENST00000262407.5:c.3060+2T=	ENSP00000262407.5:n.3060+2T=
ENST00000587295.5:c.253+1481T=
ENST00000588098.1:c.37+307T=
ENST00000592462.5:n.2761T=
ENST00000648408.1:c.2374+307T=
XM_011524749.1:c.2958+2T=	XP_011523051.1:n.2958+2T=
XM_011524750.1:c.2943+307T=	XP_011523052.1:n.2943+307T=