Canonical Allele Identifier: CA2261367765
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44379692C= , CM000679.2:g.44379692C= GRCh38
NC_000017.10:g.42457060C= , CM000679.1:g.42457060C= GRCh37
NC_000017.9:g.39812586C= NCBI36
NG_008331.1:g.14814G= , LRG_479:g.14814G=

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.1875G= MANE Select ENSP00000262407.5:p.Glu625=
ENST00000648408.1:c.1306G=
ENST00000262407.5:c.1875G= ENSP00000262407.5:p.Glu625=
ENST00000592462.5:n.670G=
NM_000419.3:c.1875G= , LRG_479t1:c.1875G= NP_000410.2:p.Glu625=
XM_011524749.1:c.1875G= XP_011523051.1:p.Glu625=
XM_011524750.1:c.1875G= XP_011523052.1:p.Glu625=
NM_000419.4:c.1875G= NP_000410.2:p.Glu625=
NM_000419.5:c.1875G= MANE Select NP_000410.2:p.Glu625=