Canonical Allele Identifier: CA399804768

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44383931C>A , CM000679.2:g.44383931C>A	GRCh38
NC_000017.10:g.42461299C>A , CM000679.1:g.42461299C>A	GRCh37
NC_000017.9:g.39816825C>A	NCBI36
NG_008331.1:g.10575G>T , LRG_479:g.10575G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000419.5:c.961G>T MANE Select	NP_000410.2:p.Gly321Trp
ENST00000262407.6:c.961G>T MANE Select	ENSP00000262407.5:p.Gly321Trp
NM_000419.3:c.961G>T , LRG_479t1:c.961G>T	NP_000410.2:p.Gly321Trp
NM_000419.4:c.961G>T	NP_000410.2:p.Gly321Trp
ENST00000262407.5:c.961G>T	ENSP00000262407.5:p.Gly321Trp
ENST00000589645.5:n.412G>T
ENST00000591990.5:n.506G>T
ENST00000592226.5:n.201G>T
ENST00000648408.1:c.392G>T
XM_011524749.1:c.961G>T	XP_011523051.1:p.Gly321Trp
XM_011524750.1:c.961G>T	XP_011523052.1:p.Gly321Trp