Canonical Allele Identifier: CA2261368365

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44380927C= , CM000679.2:g.44380927C=	GRCh38
NC_000017.10:g.42458295C= , CM000679.1:g.42458295C=	GRCh37
NC_000017.9:g.39813821C=	NCBI36
NG_008331.1:g.13579G= , LRG_479:g.13579G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.1345G= MANE Select	ENSP00000262407.5:p.Gly449=
ENST00000648408.1:c.776G=
ENST00000262407.5:c.1345G=	ENSP00000262407.5:p.Gly449=
ENST00000592226.5:n.585G=
ENST00000592462.5:n.140G=
NM_000419.3:c.1345G= , LRG_479t1:c.1345G=	NP_000410.2:p.Gly449=
XM_011524749.1:c.1345G=	XP_011523051.1:p.Gly449=
XM_011524750.1:c.1345G=	XP_011523052.1:p.Gly449=
NM_000419.4:c.1345G=	NP_000410.2:p.Gly449=
NM_000419.5:c.1345G= MANE Select	NP_000410.2:p.Gly449=