Canonical Allele Identifier: CA2261369982

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44384493C= , CM000679.2:g.44384493C=	GRCh38
NC_000017.10:g.42461861C= , CM000679.1:g.42461861C=	GRCh37
NC_000017.9:g.39817387C=	NCBI36
NG_008331.1:g.10013G= , LRG_479:g.10013G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.847+45G= MANE Select	ENSP00000262407.5:n.847+45G=
ENST00000648408.1:c.278+45G=
ENST00000262407.5:c.847+45G=	ENSP00000262407.5:n.847+45G=
ENST00000589645.5:n.298+45G=
ENST00000591990.5:n.254G=
ENST00000592075.5:n.216+45G=
ENST00000592226.5:n.87+45G=
ENST00000592253.5:n.355+45G=
ENST00000592944.1:n.529+45G=
NM_000419.3:c.847+45G= , LRG_479t1:c.847+45G=	NP_000410.2:n.847+45G=
XM_011524749.1:c.847+45G=	XP_011523051.1:n.847+45G=
XM_011524750.1:c.847+45G=	XP_011523052.1:n.847+45G=
NM_000419.4:c.847+45G=	NP_000410.2:n.847+45G=
NM_000419.5:c.847+45G= MANE Select	NP_000410.2:n.847+45G=