Canonical Allele Identifier: CA913203486
Gene: ITGA2B HGNC NCBI

Linked Data

ClinVar Variation Id: 953035
ClinVar RCV Id: RCV001225271
dbSNP Id: rs2048678902

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44389385del , CM000679.2:g.44389385del GRCh38
NC_000017.10:g.42466753del , CM000679.1:g.42466753del GRCh37
NC_000017.9:g.39822279del NCBI36
NG_008331.1:g.5123del , LRG_479:g.5123del

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.91del MANE Select ENSP00000262407.5:p.Ala31ProfsTer2
ENST00000262407.5:c.91del ENSP00000262407.5:p.Ala31ProfsTer2
NM_000419.3:c.91del , LRG_479t1:c.91del NP_000410.2:p.Ala31ProfsTer2
XM_011524749.1:c.91del XP_011523051.1:p.Ala31ProfsTer2
XM_011524750.1:c.91del XP_011523052.1:p.Ala31ProfsTer2
NM_000419.4:c.91del NP_000410.2:p.Ala31ProfsTer2
NM_000419.5:c.91del MANE Select NP_000410.2:p.Ala31ProfsTer2