Canonical Allele Identifier: CA2638212838
Gene: ITGA2B HGNC NCBI

Linked Data

gnomAD v4: 17-44372502-CTA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372504_44372505del , CM000679.2:g.44372504_44372505del GRCh38
NC_000017.10:g.42449872_42449873del , CM000679.1:g.42449872_42449873del GRCh37
NC_000017.9:g.39805398_39805399del NCBI36
NG_008331.1:g.22002_22003del , LRG_479:g.22002_22003del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3061-81_3061-80del MANE Select ENSP00000262407.5:n.3061-81_3061-80del
ENST00000648408.1:c.2375-81_2375-80del
ENST00000262407.5:c.3061-81_3061-80del ENSP00000262407.5:n.3061-81_3061-80del
ENST00000587295.5:c.254-81_254-80del
ENST00000588098.1:c.38-81_38-80del
NM_000419.3:c.3061-81_3061-80del , LRG_479t1:c.3061-81_3061-80del NP_000410.2:n.3061-81_3061-80del
XM_011524749.1:c.2959-81_2959-80del XP_011523051.1:n.2959-81_2959-80del
XM_011524750.1:c.2944-81_2944-80del XP_011523052.1:n.2944-81_2944-80del
NM_000419.4:c.3061-81_3061-80del NP_000410.2:n.3061-81_3061-80del
NM_000419.5:c.3061-81_3061-80del MANE Select NP_000410.2:n.3061-81_3061-80del
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