Canonical Allele Identifier: CA399805055

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44384543G>A , CM000679.2:g.44384543G>A	GRCh38
NC_000017.10:g.42461911G>A , CM000679.1:g.42461911G>A	GRCh37
NC_000017.9:g.39817437G>A	NCBI36
NG_008331.1:g.9963C>T , LRG_479:g.9963C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000419.5:c.842C>T MANE Select	NP_000410.2:p.Thr281Ile
ENST00000262407.6:c.842C>T MANE Select	ENSP00000262407.5:p.Thr281Ile
NM_000419.3:c.842C>T , LRG_479t1:c.842C>T	NP_000410.2:p.Thr281Ile
NM_000419.4:c.842C>T	NP_000410.2:p.Thr281Ile
ENST00000262407.5:c.842C>T	ENSP00000262407.5:p.Thr281Ile
ENST00000589645.5:n.293C>T
ENST00000591990.5:n.204C>T
ENST00000592075.5:n.211C>T
ENST00000592226.5:n.82C>T
ENST00000592253.5:n.350C>T
ENST00000592944.1:n.524C>T
ENST00000648408.1:c.273C>T
XM_011524749.1:c.842C>T	XP_011523051.1:p.Thr281Ile
XM_011524750.1:c.842C>T	XP_011523052.1:p.Thr281Ile