Canonical Allele Identifier: CA2576290887
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44374610del , CM000679.2:g.44374610del GRCh38
NC_000017.10:g.42451978del , CM000679.1:g.42451978del GRCh37
NC_000017.9:g.39807504del NCBI36
NG_008331.1:g.19900del , LRG_479:g.19900del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.2943+53del MANE Select ENSP00000262407.5:n.2943+53del
ENST00000648408.1:c.2374+53del
ENST00000262407.5:c.2943+53del ENSP00000262407.5:n.2943+53del
ENST00000587295.5:c.253+1227del
ENST00000588098.1:c.37+53del
ENST00000592462.5:n.2507del
NM_000419.3:c.2943+53del , LRG_479t1:c.2943+53del NP_000410.2:n.2943+53del
XM_011524749.1:c.2842-136del XP_011523051.1:n.2842-136del
XM_011524750.1:c.2943+53del XP_011523052.1:n.2943+53del
NM_000419.4:c.2943+53del NP_000410.2:n.2943+53del
NM_000419.5:c.2943+53del MANE Select NP_000410.2:n.2943+53del