Canonical Allele Identifier: CA913189248
Gene: ITGA2B HGNC NCBI

Linked Data

ClinVar Variation Id: 953057
dbSNP Id: rs2048521625

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44374451del , CM000679.2:g.44374451del GRCh38
NC_000017.10:g.42451819del , CM000679.1:g.42451819del GRCh37
NC_000017.9:g.39807345del NCBI36
NG_008331.1:g.20057del , LRG_479:g.20057del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.2965del MANE Select ENSP00000262407.5:p.Ala989ProfsTer?
ENST00000648408.1:c.2374+210del
ENST00000262407.5:c.2965del ENSP00000262407.5:p.Ala989ProfsTer?
ENST00000587295.5:c.253+1384del
ENST00000588098.1:c.37+210del
ENST00000592462.5:n.2664del
NM_000419.3:c.2965del , LRG_479t1:c.2965del NP_000410.2:p.Ala989ProfsTer?
XM_011524749.1:c.2863del XP_011523051.1:p.Ala955ProfsTer?
XM_011524750.1:c.2943+210del XP_011523052.1:n.2943+210del
NM_000419.4:c.2965del NP_000410.2:p.Ala989ProfsTer?
NM_000419.5:c.2965del MANE Select NP_000410.2:p.Ala989ProfsTer?