Canonical Allele Identifier: CA2261370299

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44385121T= , CM000679.2:g.44385121T=	GRCh38
NC_000017.10:g.42462489T= , CM000679.1:g.42462489T=	GRCh37
NC_000017.9:g.39818015T=	NCBI36
NG_008331.1:g.9385A= , LRG_479:g.9385A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.670+43A= MANE Select	ENSP00000262407.5:n.670+43A=
ENST00000648408.1:c.101+43A=
ENST00000262407.5:c.670+43A=	ENSP00000262407.5:n.670+43A=
ENST00000589645.5:n.121+43A=
ENST00000591990.5:n.32+43A=
ENST00000592075.5:n.39+43A=
ENST00000592226.5:n.39+43A=
ENST00000592253.5:n.178+43A=
ENST00000592944.1:n.352+43A=
NM_000419.3:c.670+43A= , LRG_479t1:c.670+43A=	NP_000410.2:n.670+43A=
XM_011524749.1:c.670+43A=	XP_011523051.1:n.670+43A=
XM_011524750.1:c.670+43A=	XP_011523052.1:n.670+43A=
NM_000419.4:c.670+43A=	NP_000410.2:n.670+43A=
NM_000419.5:c.670+43A= MANE Select	NP_000410.2:n.670+43A=