Canonical Allele Identifier: CA915940756

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44372391dup , CM000679.2:g.44372391dup	GRCh38
NC_000017.10:g.42449759dup , CM000679.1:g.42449759dup	GRCh37
NC_000017.9:g.39805285dup	NCBI36
NG_008331.1:g.22116dup , LRG_479:g.22116dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.3094dup MANE Select	ENSP00000262407.5:p.Glu1032GlyfsTer4
ENST00000648408.1:c.2408dup
ENST00000262407.5:c.3094dup	ENSP00000262407.5:p.Glu1032GlyfsTer4
ENST00000587295.5:c.287dup
ENST00000588098.1:c.71dup
NM_000419.3:c.3094dup , LRG_479t1:c.3094dup	NP_000410.2:p.Glu1032GlyfsTer4
XM_011524749.1:c.2992dup	XP_011523051.1:p.Glu998GlyfsTer4
XM_011524750.1:c.2977dup	XP_011523052.1:p.Glu993GlyfsTer4
NM_000419.4:c.3094dup	NP_000410.2:p.Glu1032GlyfsTer4
NM_000419.5:c.3094dup MANE Select	NP_000410.2:p.Glu1032GlyfsTer4