Canonical Allele Identifier: CA2261364375
Gene: ITGA2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372425_44372426delinsTG , CM000679.2:g.44372425_44372426delinsTG GRCh38
NC_000017.10:g.42449793_42449794delinsTG , CM000679.1:g.42449793_42449794delinsTG GRCh37
NC_000017.9:g.39805319_39805320delinsTG NCBI36
NG_008331.1:g.22080_22081delinsCA , LRG_479:g.22080_22081delinsCA

Transcript Alleles

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