Canonical Allele Identifier: CA2261364420
Gene: ITGA2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372505_44372518delinsTGAGCACCTCCCTG , CM000679.2:g.44372505_44372518delinsTGAGCACCTCCCTG GRCh38
NC_000017.10:g.42449873_42449886delinsTGAGCACCTCCCTG , CM000679.1:g.42449873_42449886delinsTGAGCACCTCCCTG GRCh37
NC_000017.9:g.39805399_39805412delinsTGAGCACCTCCCTG NCBI36
NG_008331.1:g.21988_22001delinsCAGGGAGGTGCTCA , LRG_479:g.21988_22001delinsCAGGGAGGTGCTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3061-95_3061-82delinsCAGGGAGGTGCTCA MANE Select ENSP00000262407.5:n.3061-95_3061-82delinsCAGGGAGGTGCTCA
ENST00000648408.1:c.2375-95_2375-82delinsCAGGGAGGTGCTCA
ENST00000262407.5:c.3061-95_3061-82delinsCAGGGAGGTGCTCA ENSP00000262407.5:n.3061-95_3061-82delinsCAGGGAGGTGCTCA
ENST00000587295.5:c.254-95_254-82delinsCAGGGAGGTGCTCA
ENST00000588098.1:c.38-95_38-82delinsCAGGGAGGTGCTCA
NM_000419.3:c.3061-95_3061-82delinsCAGGGAGGTGCTCA , LRG_479t1:c.3061-95_3061-82delinsCAGGGAGGTGCTCA NP_000410.2:n.3061-95_3061-82delinsCAGGGAGGTGCTCA
XM_011524749.1:c.2959-95_2959-82delinsCAGGGAGGTGCTCA XP_011523051.1:n.2959-95_2959-82delinsCAGGGAGGTGCTCA
XM_011524750.1:c.2944-95_2944-82delinsCAGGGAGGTGCTCA XP_011523052.1:n.2944-95_2944-82delinsCAGGGAGGTGCTCA
NM_000419.4:c.3061-95_3061-82delinsCAGGGAGGTGCTCA NP_000410.2:n.3061-95_3061-82delinsCAGGGAGGTGCTCA
NM_000419.5:c.3061-95_3061-82delinsCAGGGAGGTGCTCA MANE Select NP_000410.2:n.3061-95_3061-82delinsCAGGGAGGTGCTCA
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