Canonical Allele Identifier: CA2261369847
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44384227G= , CM000679.2:g.44384227G= GRCh38
NC_000017.10:g.42461595G= , CM000679.1:g.42461595G= GRCh37
NC_000017.9:g.39817121G= NCBI36
NG_008331.1:g.10279C= , LRG_479:g.10279C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.891+84C= MANE Select ENSP00000262407.5:n.891+84C=
ENST00000648408.1:c.322+84C=
ENST00000262407.5:c.891+84C= ENSP00000262407.5:n.891+84C=
ENST00000589645.5:n.342+84C=
ENST00000591990.5:n.436+84C=
ENST00000592075.5:n.260+84C=
ENST00000592226.5:n.131+84C=
ENST00000592253.5:n.399+84C=
NM_000419.3:c.891+84C= , LRG_479t1:c.891+84C= NP_000410.2:n.891+84C=
XM_011524749.1:c.891+84C= XP_011523051.1:n.891+84C=
XM_011524750.1:c.891+84C= XP_011523052.1:n.891+84C=
NM_000419.4:c.891+84C= NP_000410.2:n.891+84C=
NM_000419.5:c.891+84C= MANE Select NP_000410.2:n.891+84C=