Canonical Allele Identifier: CA983994159
Gene: ITGA2B HGNC NCBI

Linked Data

dbSNP Id: rs1160599771
gnomAD v3: 17-44372639-CT-C
gnomAD v4: 17-44372639-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372647del , CM000679.2:g.44372647del GRCh38
NC_000017.10:g.42450015del , CM000679.1:g.42450015del GRCh37
NC_000017.9:g.39805541del NCBI36
NG_008331.1:g.21866del , LRG_479:g.21866del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3061-217del MANE Select ENSP00000262407.5:n.3061-217del
ENST00000648408.1:c.2375-217del
ENST00000262407.5:c.3061-217del ENSP00000262407.5:n.3061-217del
ENST00000587295.5:c.254-217del
ENST00000588098.1:c.38-217del
NM_000419.3:c.3061-217del , LRG_479t1:c.3061-217del NP_000410.2:n.3061-217del
XM_011524749.1:c.2959-217del XP_011523051.1:n.2959-217del
XM_011524750.1:c.2944-217del XP_011523052.1:n.2944-217del
NM_000419.4:c.3061-217del NP_000410.2:n.3061-217del
NM_000419.5:c.3061-217del MANE Select NP_000410.2:n.3061-217del
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