Canonical Allele Identifier: CA2261366900

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44377786A= , CM000679.2:g.44377786A=	GRCh38
NC_000017.10:g.42455154A= , CM000679.1:g.42455154A=	GRCh37
NC_000017.9:g.39810680A=	NCBI36
NG_008331.1:g.16720T= , LRG_479:g.16720T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2099T= MANE Select	ENSP00000262407.5:p.Phe700=
ENST00000648408.1:c.1530T=
ENST00000262407.5:c.2099T=	ENSP00000262407.5:p.Phe700=
ENST00000592462.5:n.894T=
NM_000419.3:c.2099T= , LRG_479t1:c.2099T=	NP_000410.2:p.Phe700=
XM_011524749.1:c.2099T=	XP_011523051.1:p.Phe700=
XM_011524750.1:c.2099T=	XP_011523052.1:p.Phe700=
NM_000419.4:c.2099T=	NP_000410.2:p.Phe700=
NM_000419.5:c.2099T= MANE Select	NP_000410.2:p.Phe700=