Canonical Allele Identifier: CA8603306

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44384316C>T , CM000679.2:g.44384316C>T	GRCh38
NC_000017.10:g.42461684C>T , CM000679.1:g.42461684C>T	GRCh37
NC_000017.9:g.39817210C>T	NCBI36
NG_008331.1:g.10190G>A , LRG_479:g.10190G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000419.5:c.886G>A MANE Select	NP_000410.2:p.Gly296Arg
ENST00000262407.6:c.886G>A MANE Select	ENSP00000262407.5:p.Gly296Arg
NM_000419.3:c.886G>A , LRG_479t1:c.886G>A	NP_000410.2:p.Gly296Arg
NM_000419.4:c.886G>A	NP_000410.2:p.Gly296Arg
ENST00000262407.5:c.886G>A	ENSP00000262407.5:p.Gly296Arg
ENST00000589645.5:n.337G>A
ENST00000591990.5:n.431G>A
ENST00000592075.5:n.255G>A
ENST00000592226.5:n.126G>A
ENST00000592253.5:n.394G>A
ENST00000648408.1:c.317G>A
XM_011524749.1:c.886G>A	XP_011523051.1:p.Gly296Arg
XM_011524750.1:c.886G>A	XP_011523052.1:p.Gly296Arg