Canonical Allele Identifier: CA8623018
Gene: ITGB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2919628
dbSNP Id: rs776647833

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47286308G>A , CM000679.2:g.47286308G>A GRCh38
NC_000017.10:g.45363674G>A , CM000679.1:g.45363674G>A GRCh37
NC_000017.9:g.42718673G>A NCBI36
NG_008332.2:g.37467G>A , LRG_481:g.37467G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.663G>A ENSP00000513002.1:p.Thr221=
ENST00000559488.7:c.663G>A MANE Select ENSP00000452786.2:p.Thr221=
ENST00000559488.5:c.663G>A ENSP00000452786.1:p.Thr221=
ENST00000560629.1:c.628G>A
ENST00000571680.1:c.663G>A ENSP00000461626.1:p.Thr221=
NM_000212.2:c.663G>A , LRG_481t1:c.663G>A NP_000203.2:p.Thr221=
NM_000212.3:c.663G>A MANE Select NP_000203.2:p.Thr221=