Canonical Allele Identifier: CA2809589680
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372466del , CM000679.2:g.44372466del GRCh38
NC_000017.10:g.42449834del , CM000679.1:g.42449834del GRCh37
NC_000017.9:g.39805360del NCBI36
NG_008331.1:g.22042del , LRG_479:g.22042del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3061-41del MANE Select ENSP00000262407.5:n.3061-41del
ENST00000648408.1:c.2375-41del
ENST00000262407.5:c.3061-41del ENSP00000262407.5:n.3061-41del
ENST00000587295.5:c.254-41del
ENST00000588098.1:c.38-41del
NM_000419.3:c.3061-41del , LRG_479t1:c.3061-41del NP_000410.2:n.3061-41del
XM_011524749.1:c.2959-41del XP_011523051.1:n.2959-41del
XM_011524750.1:c.2944-41del XP_011523052.1:n.2944-41del
NM_000419.4:c.3061-41del NP_000410.2:n.3061-41del
NM_000419.5:c.3061-41del MANE Select NP_000410.2:n.3061-41del