Canonical Allele Identifier: CA2261364284
Gene: ITGA2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372241_44372242delinsGA , CM000679.2:g.44372241_44372242delinsGA GRCh38
NC_000017.10:g.42449609_42449610delinsGA , CM000679.1:g.42449609_42449610delinsGA GRCh37
NC_000017.9:g.39805135_39805136delinsGA NCBI36
NG_008331.1:g.22264_22265delinsTC , LRG_479:g.22264_22265delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.*122_*123delinsTC MANE Select ENSP00000262407.5:n.*122_*123delinsTC
ENST00000648408.1:c.2556_2557delinsTC
ENST00000262407.5:c.*122_*123delinsTC ENSP00000262407.5:n.*122_*123delinsTC
ENST00000587295.5:c.435_436delinsTC
ENST00000588098.1:c.219_220delinsTC
NM_000419.3:c.*122_*123delinsTC , LRG_479t1:c.*122_*123delinsTC NP_000410.2:n.*122_*123delinsTC
XM_011524749.1:c.*122_*123delinsTC XP_011523051.1:n.*122_*123delinsTC
XM_011524750.1:c.*122_*123delinsTC XP_011523052.1:n.*122_*123delinsTC
NM_000419.4:c.*122_*123delinsTC NP_000410.2:n.*122_*123delinsTC
NM_000419.5:c.*122_*123delinsTC MANE Select NP_000410.2:n.*122_*123delinsTC
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