Canonical Allele Identifier: CA2838226999

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374837dup , CM000679.2:g.44374837dup	GRCh38
NC_000017.10:g.42452205dup , CM000679.1:g.42452205dup	GRCh37
NC_000017.9:g.39807731dup	NCBI36
NG_008331.1:g.19673dup , LRG_479:g.19673dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2842-73dup MANE Select	ENSP00000262407.5:n.2842-73dup
ENST00000648408.1:c.2273-73dup
ENST00000262407.5:c.2842-73dup	ENSP00000262407.5:n.2842-73dup
ENST00000587295.5:c.253+1000dup
ENST00000592462.5:n.2280dup
NM_000419.3:c.2842-73dup , LRG_479t1:c.2842-73dup	NP_000410.2:n.2842-73dup
XM_011524749.1:c.2841+165dup	XP_011523051.1:n.2841+165dup
XM_011524750.1:c.2842-73dup	XP_011523052.1:n.2842-73dup
NM_000419.4:c.2842-73dup	NP_000410.2:n.2842-73dup
NM_000419.5:c.2842-73dup MANE Select	NP_000410.2:n.2842-73dup