Canonical Allele Identifier: CA2840405145

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44379677dup , CM000679.2:g.44379677dup	GRCh38
NC_000017.10:g.42457045dup , CM000679.1:g.42457045dup	GRCh37
NC_000017.9:g.39812571dup	NCBI36
NG_008331.1:g.14829dup , LRG_479:g.14829dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.1878+12dup MANE Select	ENSP00000262407.5:n.1878+12dup
ENST00000648408.1:c.1309+12dup
ENST00000262407.5:c.1878+12dup	ENSP00000262407.5:n.1878+12dup
ENST00000592462.5:n.673+12dup
NM_000419.3:c.1878+12dup , LRG_479t1:c.1878+12dup	NP_000410.2:n.1878+12dup
XM_011524749.1:c.1878+12dup	XP_011523051.1:n.1878+12dup
XM_011524750.1:c.1878+12dup	XP_011523052.1:n.1878+12dup
NM_000419.4:c.1878+12dup	NP_000410.2:n.1878+12dup
NM_000419.5:c.1878+12dup MANE Select	NP_000410.2:n.1878+12dup