Canonical Allele Identifier: CA2261364481
Gene: ITGA2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372663_44372665delinsCTG , CM000679.2:g.44372663_44372665delinsCTG GRCh38
NC_000017.10:g.42450031_42450033delinsCTG , CM000679.1:g.42450031_42450033delinsCTG GRCh37
NC_000017.9:g.39805557_39805559delinsCTG NCBI36
NG_008331.1:g.21841_21843delinsCAG , LRG_479:g.21841_21843delinsCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3061-242_3061-240delinsCAG MANE Select ENSP00000262407.5:n.3061-242_3061-240delinsCAG
ENST00000648408.1:c.2375-242_2375-240delinsCAG
ENST00000262407.5:c.3061-242_3061-240delinsCAG ENSP00000262407.5:n.3061-242_3061-240delinsCAG
ENST00000587295.5:c.254-242_254-240delinsCAG
ENST00000588098.1:c.38-242_38-240delinsCAG
NM_000419.3:c.3061-242_3061-240delinsCAG , LRG_479t1:c.3061-242_3061-240delinsCAG NP_000410.2:n.3061-242_3061-240delinsCAG
XM_011524749.1:c.2959-242_2959-240delinsCAG XP_011523051.1:n.2959-242_2959-240delinsCAG
XM_011524750.1:c.2944-242_2944-240delinsCAG XP_011523052.1:n.2944-242_2944-240delinsCAG
NM_000419.4:c.3061-242_3061-240delinsCAG NP_000410.2:n.3061-242_3061-240delinsCAG
NM_000419.5:c.3061-242_3061-240delinsCAG MANE Select NP_000410.2:n.3061-242_3061-240delinsCAG
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