Canonical Allele Identifier: CA2261367773
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44379713A= , CM000679.2:g.44379713A= GRCh38
NC_000017.10:g.42457081A= , CM000679.1:g.42457081A= GRCh37
NC_000017.9:g.39812607A= NCBI36
NG_008331.1:g.14793T= , LRG_479:g.14793T=

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.1854T= MANE Select ENSP00000262407.5:p.His618=
ENST00000648408.1:c.1285T=
ENST00000262407.5:c.1854T= ENSP00000262407.5:p.His618=
ENST00000592462.5:n.649T=
NM_000419.3:c.1854T= , LRG_479t1:c.1854T= NP_000410.2:p.His618=
XM_011524749.1:c.1854T= XP_011523051.1:p.His618=
XM_011524750.1:c.1854T= XP_011523052.1:p.His618=
NM_000419.4:c.1854T= NP_000410.2:p.His618=
NM_000419.5:c.1854T= MANE Select NP_000410.2:p.His618=