Canonical Allele Identifier: CA2261364449
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372583T= , CM000679.2:g.44372583T= GRCh38
NC_000017.10:g.42449951T= , CM000679.1:g.42449951T= GRCh37
NC_000017.9:g.39805477T= NCBI36
NG_008331.1:g.21923A= , LRG_479:g.21923A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3061-160A= MANE Select ENSP00000262407.5:n.3061-160A=
ENST00000648408.1:c.2375-160A=
ENST00000262407.5:c.3061-160A= ENSP00000262407.5:n.3061-160A=
ENST00000587295.5:c.254-160A=
ENST00000588098.1:c.38-160A=
NM_000419.3:c.3061-160A= , LRG_479t1:c.3061-160A= NP_000410.2:n.3061-160A=
XM_011524749.1:c.2959-160A= XP_011523051.1:n.2959-160A=
XM_011524750.1:c.2944-160A= XP_011523052.1:n.2944-160A=
NM_000419.4:c.3061-160A= NP_000410.2:n.3061-160A=
NM_000419.5:c.3061-160A= MANE Select NP_000410.2:n.3061-160A=