Canonical Allele Identifier: CA772284372
Gene: ITGA2B HGNC NCBI

Linked Data

dbSNP Id: rs796401871
gnomAD v3: 17-44372212-AG-A
gnomAD v4: 17-44372212-AG-A
MyVariant Identifiers: chr17:g.42449581del (hg19) chr17:g.44372213del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372219del , CM000679.2:g.44372219del GRCh38
NC_000017.10:g.42449587del , CM000679.1:g.42449587del GRCh37
NC_000017.9:g.39805113del NCBI36
NG_008331.1:g.22293del , LRG_479:g.22293del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.*151del MANE Select ENSP00000262407.5:n.*151del
ENST00000648408.1:c.2585del
ENST00000262407.5:c.*151del ENSP00000262407.5:n.*151del
ENST00000587295.5:c.464del
ENST00000588098.1:c.248del
NM_000419.3:c.*151del , LRG_479t1:c.*151del NP_000410.2:n.*151del
XM_011524749.1:c.*151del XP_011523051.1:n.*151del
XM_011524750.1:c.*151del XP_011523052.1:n.*151del
NM_000419.4:c.*151del NP_000410.2:n.*151del
NM_000419.5:c.*151del MANE Select NP_000410.2:n.*151del
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