Canonical Allele Identifier: CA2261364458
Gene: ITGA2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372600_44372602delinsTGG , CM000679.2:g.44372600_44372602delinsTGG GRCh38
NC_000017.10:g.42449968_42449970delinsTGG , CM000679.1:g.42449968_42449970delinsTGG GRCh37
NC_000017.9:g.39805494_39805496delinsTGG NCBI36
NG_008331.1:g.21904_21906delinsCCA , LRG_479:g.21904_21906delinsCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3061-179_3061-177delinsCCA MANE Select ENSP00000262407.5:n.3061-179_3061-177delinsCCA
ENST00000648408.1:c.2375-179_2375-177delinsCCA
ENST00000262407.5:c.3061-179_3061-177delinsCCA ENSP00000262407.5:n.3061-179_3061-177delinsCCA
ENST00000587295.5:c.254-179_254-177delinsCCA
ENST00000588098.1:c.38-179_38-177delinsCCA
NM_000419.3:c.3061-179_3061-177delinsCCA , LRG_479t1:c.3061-179_3061-177delinsCCA NP_000410.2:n.3061-179_3061-177delinsCCA
XM_011524749.1:c.2959-179_2959-177delinsCCA XP_011523051.1:n.2959-179_2959-177delinsCCA
XM_011524750.1:c.2944-179_2944-177delinsCCA XP_011523052.1:n.2944-179_2944-177delinsCCA
NM_000419.4:c.3061-179_3061-177delinsCCA NP_000410.2:n.3061-179_3061-177delinsCCA
NM_000419.5:c.3061-179_3061-177delinsCCA MANE Select NP_000410.2:n.3061-179_3061-177delinsCCA
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