Canonical Allele Identifier: CA645584247
Gene: ITGA2B HGNC NCBI

Linked Data

gnomAD v4: 17-44372420-CG-C
COSMIC: COSM4747077
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372421del , CM000679.2:g.44372421del GRCh38
NC_000017.10:g.42449789del , CM000679.1:g.42449789del GRCh37
NC_000017.9:g.39805315del NCBI36
NG_008331.1:g.22085del , LRG_479:g.22085del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3063del MANE Select ENSP00000262407.5:p.Gly1022AlafsTer?
ENST00000648408.1:c.2377del
ENST00000262407.5:c.3063del ENSP00000262407.5:p.Gly1022AlafsTer?
ENST00000587295.5:c.256del
ENST00000588098.1:c.40del
NM_000419.3:c.3063del , LRG_479t1:c.3063del NP_000410.2:p.Gly1022AlafsTer?
XM_011524749.1:c.2961del XP_011523051.1:p.Gly988AlafsTer?
XM_011524750.1:c.2946del XP_011523052.1:p.Gly983AlafsTer?
NM_000419.4:c.3063del NP_000410.2:p.Gly1022AlafsTer?
NM_000419.5:c.3063del MANE Select NP_000410.2:p.Gly1022AlafsTer?
Search 100 bp 5'
Search 100 bp 3'