Canonical Allele Identifier: CA2809589684
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372561_44372562insGCAGCATGCTCAGCATCAGGGCTCAGTCTCTTTATTAGGCAGCAGGAGGGGGGGTAGCCCAGCT , CM000679.2:g.44372561_44372562insGCAGCATGCTCAGCATCAGGGCTCAGTCTCTTTATTAGGCAGCAGGAGGGGGGGTAGCCCAGCT GRCh38
NC_000017.10:g.42449929_42449930insGCAGCATGCTCAGCATCAGGGCTCAGTCTCTTTATTAGGCAGCAGGAGGGGGGGTAGCCCAGCT , CM000679.1:g.42449929_42449930insGCAGCATGCTCAGCATCAGGGCTCAGTCTCTTTATTAGGCAGCAGGAGGGGGGGTAGCCCAGCT GRCh37
NC_000017.9:g.39805455_39805456insGCAGCATGCTCAGCATCAGGGCTCAGTCTCTTTATTAGGCAGCAGGAGGGGGGGTAGCCCAGCT NCBI36
NG_008331.1:g.21944_21945insAGCTGGGCTACCCCCCCTCCTGCTGCCTAATAAAGAGACTGAGCCCTGATGCTGAGCATGCTGC , LRG_479:g.21944_21945insAGCTGGGCTACCCCCCCTCCTGCTGCCTAATAAAGAGACTGAGCCCTGATGCTGAGCATGCTGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3061-139_3061-138insAGCTGGGCTACCCCCCCTCCTGCTGCCTAATAAAGAGACTGAGCCCTGATGCTGAGCATGCTGC MANE Select ENSP00000262407.5:n.3061-139_3061-138insAGCTGGGCTACCCCCCCTCCT...
ENST00000648408.1:c.2375-139_2375-138insAGCTGGGCTACCCCCCCTCCTGCTGCCTAATAAAGAGACTGAGCCCTGATGCTGAGCATGCTGC
ENST00000262407.5:c.3061-139_3061-138insAGCTGGGCTACCCCCCCTCCTGCTGCCTAATAAAGAGACTGAGCCCTGATGCTGAGCATGCTGC ENSP00000262407.5:n.3061-139_3061-138insAGCTGGGCTACCCCCCCTCCT...
ENST00000587295.5:c.254-139_254-138insAGCTGGGCTACCCCCCCTCCTGCTGCCTAATAAAGAGACTGAGCCCTGATGCTGAGCATGCTGC
ENST00000588098.1:c.38-139_38-138insAGCTGGGCTACCCCCCCTCCTGCTGCCTAATAAAGAGACTGAGCCCTGATGCTGAGCATGCTGC
NM_000419.3:c.3061-139_3061-138insAGCTGGGCTACCCCCCCTCCTGCTGCCTAATAAAGAGACTGAGCCCTGATGCTGAGCATGCTGC , LRG_479t1:c.3061-139_3061-138insAGCTGGGCTACCCCCCCTCCTGCTGCCTAATAAAGAGACTGAGCCCTGATGCTGAGCATGCTGC NP_000410.2:n.3061-139_3061-138insAGCTGGGCTACCCCCCCTCCTGCTGCC...
XM_011524749.1:c.2959-139_2959-138insAGCTGGGCTACCCCCCCTCCTGCTGCCTAATAAAGAGACTGAGCCCTGATGCTGAGCATGCTGC XP_011523051.1:n.2959-139_2959-138insAGCTGGGCTACCCCCCCTCCTGCT...
XM_011524750.1:c.2944-139_2944-138insAGCTGGGCTACCCCCCCTCCTGCTGCCTAATAAAGAGACTGAGCCCTGATGCTGAGCATGCTGC XP_011523052.1:n.2944-139_2944-138insAGCTGGGCTACCCCCCCTCCTGCT...
NM_000419.4:c.3061-139_3061-138insAGCTGGGCTACCCCCCCTCCTGCTGCCTAATAAAGAGACTGAGCCCTGATGCTGAGCATGCTGC NP_000410.2:n.3061-139_3061-138insAGCTGGGCTACCCCCCCTCCTGCTGCC...
NM_000419.5:c.3061-139_3061-138insAGCTGGGCTACCCCCCCTCCTGCTGCCTAATAAAGAGACTGAGCCCTGATGCTGAGCATGCTGC MANE Select NP_000410.2:n.3061-139_3061-138insAGCTGGGCTACCCCCCCTCCTGCTGCC...