Canonical Allele Identifier: CA2261364298

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44372264T= , CM000679.2:g.44372264T=	GRCh38
NC_000017.10:g.42449632T= , CM000679.1:g.42449632T=	GRCh37
NC_000017.9:g.39805158T=	NCBI36
NG_008331.1:g.22242A= , LRG_479:g.22242A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.*100A= MANE Select	ENSP00000262407.5:n.*100A=
ENST00000648408.1:c.2534A=
ENST00000262407.5:c.*100A=	ENSP00000262407.5:n.*100A=
ENST00000587295.5:c.413A=
ENST00000588098.1:c.197A=
NM_000419.3:c.*100A= , LRG_479t1:c.*100A=	NP_000410.2:n.*100A=
XM_011524749.1:c.*100A=	XP_011523051.1:n.*100A=
XM_011524750.1:c.*100A=	XP_011523052.1:n.*100A=
NM_000419.4:c.*100A=	NP_000410.2:n.*100A=
NM_000419.5:c.*100A= MANE Select	NP_000410.2:n.*100A=