Canonical Allele Identifier: CA2638212824
Gene: ITGA2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372491_44372492insTTCCCTGAGGCCCTGCCGCCCTTTCTCCCTCTTTTCTTTTTTTTTTGAGAC , CM000679.2:g.44372491_44372492insTTCCCTGAGGCCCTGCCGCCCTTTCTCCCTCTTTTCTTTTTTTTTTGAGAC GRCh38
NC_000017.10:g.42449859_42449860insTTCCCTGAGGCCCTGCCGCCCTTTCTCCCTCTTTTCTTTTTTTTTTGAGAC , CM000679.1:g.42449859_42449860insTTCCCTGAGGCCCTGCCGCCCTTTCTCCCTCTTTTCTTTTTTTTTTGAGAC GRCh37
NC_000017.9:g.39805385_39805386insTTCCCTGAGGCCCTGCCGCCCTTTCTCCCTCTTTTCTTTTTTTTTTGAGAC NCBI36
NG_008331.1:g.22014_22015insGTCTCAAAAAAAAAAGAAAAGAGGGAGAAAGGGCGGCAGGGCCTCAGGGAA , LRG_479:g.22014_22015insGTCTCAAAAAAAAAAGAAAAGAGGGAGAAAGGGCGGCAGGGCCTCAGGGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3061-69_3061-68insGTCTCAAAAAAAAAAGAAAAGAGGGAGAAAGGGCGGCAGGGCCTCAGGGAA MANE Select ENSP00000262407.5:n.3061-69_3061-68insGTCTCAAAAAAAAAAGAAAAGAG...
ENST00000648408.1:c.2375-69_2375-68insGTCTCAAAAAAAAAAGAAAAGAGGGAGAAAGGGCGGCAGGGCCTCAGGGAA
ENST00000262407.5:c.3061-69_3061-68insGTCTCAAAAAAAAAAGAAAAGAGGGAGAAAGGGCGGCAGGGCCTCAGGGAA ENSP00000262407.5:n.3061-69_3061-68insGTCTCAAAAAAAAAAGAAAAGAG...
ENST00000587295.5:c.254-69_254-68insGTCTCAAAAAAAAAAGAAAAGAGGGAGAAAGGGCGGCAGGGCCTCAGGGAA
ENST00000588098.1:c.38-69_38-68insGTCTCAAAAAAAAAAGAAAAGAGGGAGAAAGGGCGGCAGGGCCTCAGGGAA
NM_000419.3:c.3061-69_3061-68insGTCTCAAAAAAAAAAGAAAAGAGGGAGAAAGGGCGGCAGGGCCTCAGGGAA , LRG_479t1:c.3061-69_3061-68insGTCTCAAAAAAAAAAGAAAAGAGGGAGAAAGGGCGGCAGGGCCTCAGGGAA NP_000410.2:n.3061-69_3061-68insGTCTCAAAAAAAAAAGAAAAGAGGGAGAA...
XM_011524749.1:c.2959-69_2959-68insGTCTCAAAAAAAAAAGAAAAGAGGGAGAAAGGGCGGCAGGGCCTCAGGGAA XP_011523051.1:n.2959-69_2959-68insGTCTCAAAAAAAAAAGAAAAGAGGGA...
XM_011524750.1:c.2944-69_2944-68insGTCTCAAAAAAAAAAGAAAAGAGGGAGAAAGGGCGGCAGGGCCTCAGGGAA XP_011523052.1:n.2944-69_2944-68insGTCTCAAAAAAAAAAGAAAAGAGGGA...
NM_000419.4:c.3061-69_3061-68insGTCTCAAAAAAAAAAGAAAAGAGGGAGAAAGGGCGGCAGGGCCTCAGGGAA NP_000410.2:n.3061-69_3061-68insGTCTCAAAAAAAAAAGAAAAGAGGGAGAA...
NM_000419.5:c.3061-69_3061-68insGTCTCAAAAAAAAAAGAAAAGAGGGAGAAAGGGCGGCAGGGCCTCAGGGAA MANE Select NP_000410.2:n.3061-69_3061-68insGTCTCAAAAAAAAAAGAAAAGAGGGAGAA...