Canonical Allele Identifier: CA2261369845
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44384226G= , CM000679.2:g.44384226G= GRCh38
NC_000017.10:g.42461594G= , CM000679.1:g.42461594G= GRCh37
NC_000017.9:g.39817120G= NCBI36
NG_008331.1:g.10280C= , LRG_479:g.10280C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.891+85C= MANE Select ENSP00000262407.5:n.891+85C=
ENST00000648408.1:c.322+85C=
ENST00000262407.5:c.891+85C= ENSP00000262407.5:n.891+85C=
ENST00000589645.5:n.342+85C=
ENST00000591990.5:n.436+85C=
ENST00000592075.5:n.260+85C=
ENST00000592226.5:n.131+85C=
ENST00000592253.5:n.399+85C=
NM_000419.3:c.891+85C= , LRG_479t1:c.891+85C= NP_000410.2:n.891+85C=
XM_011524749.1:c.891+85C= XP_011523051.1:n.891+85C=
XM_011524750.1:c.891+85C= XP_011523052.1:n.891+85C=
NM_000419.4:c.891+85C= NP_000410.2:n.891+85C=
NM_000419.5:c.891+85C= MANE Select NP_000410.2:n.891+85C=