Canonical Allele Identifier: CA2261365748

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44375427C= , CM000679.2:g.44375427C=	GRCh38
NC_000017.10:g.42452795C= , CM000679.1:g.42452795C=	GRCh37
NC_000017.9:g.39808321C=	NCBI36
NG_008331.1:g.19079G= , LRG_479:g.19079G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2727+164G= MANE Select	ENSP00000262407.5:n.2727+164G=
ENST00000648408.1:c.2158+164G=
ENST00000262407.5:c.2727+164G=	ENSP00000262407.5:n.2727+164G=
ENST00000587295.5:c.253+406G=
ENST00000592462.5:n.1686G=
NM_000419.3:c.2727+164G= , LRG_479t1:c.2727+164G=	NP_000410.2:n.2727+164G=
XM_011524749.1:c.2727+164G=	XP_011523051.1:n.2727+164G=
XM_011524750.1:c.2727+164G=	XP_011523052.1:n.2727+164G=
NM_000419.4:c.2727+164G=	NP_000410.2:n.2727+164G=
NM_000419.5:c.2727+164G= MANE Select	NP_000410.2:n.2727+164G=