Canonical Allele Identifier: CA2261370314
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44385145T= , CM000679.2:g.44385145T= GRCh38
NC_000017.10:g.42462513T= , CM000679.1:g.42462513T= GRCh37
NC_000017.9:g.39818039T= NCBI36
NG_008331.1:g.9361A= , LRG_479:g.9361A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.670+19A= MANE Select ENSP00000262407.5:n.670+19A=
ENST00000648408.1:c.101+19A=
ENST00000262407.5:c.670+19A= ENSP00000262407.5:n.670+19A=
ENST00000589645.5:n.121+19A=
ENST00000591990.5:n.32+19A=
ENST00000592075.5:n.39+19A=
ENST00000592226.5:n.39+19A=
ENST00000592253.5:n.178+19A=
ENST00000592944.1:n.352+19A=
NM_000419.3:c.670+19A= , LRG_479t1:c.670+19A= NP_000410.2:n.670+19A=
XM_011524749.1:c.670+19A= XP_011523051.1:n.670+19A=
XM_011524750.1:c.670+19A= XP_011523052.1:n.670+19A=
NM_000419.4:c.670+19A= NP_000410.2:n.670+19A=
NM_000419.5:c.670+19A= MANE Select NP_000410.2:n.670+19A=