Canonical Allele Identifier: CA399805011

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44384345A>T , CM000679.2:g.44384345A>T	GRCh38
NC_000017.10:g.42461713A>T , CM000679.1:g.42461713A>T	GRCh37
NC_000017.9:g.39817239A>T	NCBI36
NG_008331.1:g.10161T>A , LRG_479:g.10161T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000419.5:c.857T>A MANE Select	NP_000410.2:p.Val286Asp
ENST00000262407.6:c.857T>A MANE Select	ENSP00000262407.5:p.Val286Asp
NM_000419.3:c.857T>A , LRG_479t1:c.857T>A	NP_000410.2:p.Val286Asp
NM_000419.4:c.857T>A	NP_000410.2:p.Val286Asp
ENST00000262407.5:c.857T>A	ENSP00000262407.5:p.Val286Asp
ENST00000589645.5:n.308T>A
ENST00000591990.5:n.402T>A
ENST00000592075.5:n.226T>A
ENST00000592226.5:n.97T>A
ENST00000592253.5:n.365T>A
ENST00000592944.1:n.539T>A
ENST00000648408.1:c.288T>A
XM_011524749.1:c.857T>A	XP_011523051.1:p.Val286Asp
XM_011524750.1:c.857T>A	XP_011523052.1:p.Val286Asp