Canonical Allele Identifier: CA2261364476
Gene: ITGA2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372650_44372651delinsAG , CM000679.2:g.44372650_44372651delinsAG GRCh38
NC_000017.10:g.42450018_42450019delinsAG , CM000679.1:g.42450018_42450019delinsAG GRCh37
NC_000017.9:g.39805544_39805545delinsAG NCBI36
NG_008331.1:g.21855_21856delinsCT , LRG_479:g.21855_21856delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3061-228_3061-227delinsCT MANE Select ENSP00000262407.5:n.3061-228_3061-227delinsCT
ENST00000648408.1:c.2375-228_2375-227delinsCT
ENST00000262407.5:c.3061-228_3061-227delinsCT ENSP00000262407.5:n.3061-228_3061-227delinsCT
ENST00000587295.5:c.254-228_254-227delinsCT
ENST00000588098.1:c.38-228_38-227delinsCT
NM_000419.3:c.3061-228_3061-227delinsCT , LRG_479t1:c.3061-228_3061-227delinsCT NP_000410.2:n.3061-228_3061-227delinsCT
XM_011524749.1:c.2959-228_2959-227delinsCT XP_011523051.1:n.2959-228_2959-227delinsCT
XM_011524750.1:c.2944-228_2944-227delinsCT XP_011523052.1:n.2944-228_2944-227delinsCT
NM_000419.4:c.3061-228_3061-227delinsCT NP_000410.2:n.3061-228_3061-227delinsCT
NM_000419.5:c.3061-228_3061-227delinsCT MANE Select NP_000410.2:n.3061-228_3061-227delinsCT
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