Canonical Allele Identifier: CA2261364292
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372251C= , CM000679.2:g.44372251C= GRCh38
NC_000017.10:g.42449619C= , CM000679.1:g.42449619C= GRCh37
NC_000017.9:g.39805145C= NCBI36
NG_008331.1:g.22255G= , LRG_479:g.22255G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.*113G= MANE Select ENSP00000262407.5:n.*113G=
ENST00000648408.1:c.2547G=
ENST00000262407.5:c.*113G= ENSP00000262407.5:n.*113G=
ENST00000587295.5:c.426G=
ENST00000588098.1:c.210G=
NM_000419.3:c.*113G= , LRG_479t1:c.*113G= NP_000410.2:n.*113G=
XM_011524749.1:c.*113G= XP_011523051.1:n.*113G=
XM_011524750.1:c.*113G= XP_011523052.1:n.*113G=
NM_000419.4:c.*113G= NP_000410.2:n.*113G=
NM_000419.5:c.*113G= MANE Select NP_000410.2:n.*113G=