Canonical Allele Identifier: CA2638214842
Gene: ITGA2B HGNC NCBI

Linked Data

gnomAD v4: 17-44374605-T-TG
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44374610dup , CM000679.2:g.44374610dup GRCh38
NC_000017.10:g.42451978dup , CM000679.1:g.42451978dup GRCh37
NC_000017.9:g.39807504dup NCBI36
NG_008331.1:g.19900dup , LRG_479:g.19900dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.2943+53dup MANE Select ENSP00000262407.5:n.2943+53dup
ENST00000648408.1:c.2374+53dup
ENST00000262407.5:c.2943+53dup ENSP00000262407.5:n.2943+53dup
ENST00000587295.5:c.253+1227dup
ENST00000588098.1:c.37+53dup
ENST00000592462.5:n.2507dup
NM_000419.3:c.2943+53dup , LRG_479t1:c.2943+53dup NP_000410.2:n.2943+53dup
XM_011524749.1:c.2842-136dup XP_011523051.1:n.2842-136dup
XM_011524750.1:c.2943+53dup XP_011523052.1:n.2943+53dup
NM_000419.4:c.2943+53dup NP_000410.2:n.2943+53dup
NM_000419.5:c.2943+53dup MANE Select NP_000410.2:n.2943+53dup
Search 100 bp 5'
Search 100 bp 3'