Canonical Allele Identifier: CA2262605991
Gene: ITGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47286308_47286312delinsGCTAA , CM000679.2:g.47286308_47286312delinsGCTAA GRCh38
NC_000017.10:g.45363674_45363678delinsGCTAA , CM000679.1:g.45363674_45363678delinsGCTAA GRCh37
NC_000017.9:g.42718673_42718677delinsGCTAA NCBI36
NG_008332.2:g.37467_37471delinsGCTAA , LRG_481:g.37467_37471delinsGCTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.663_667delinsGCTAA ENSP00000513002.1:p.Thr221=
ENST00000559488.7:c.663_667delinsGCTAA MANE Select ENSP00000452786.2:p.Thr221=
ENST00000559488.5:c.663_667delinsGCTAA ENSP00000452786.1:p.Thr221=
ENST00000560629.1:c.628_632delinsGCTAA
ENST00000571680.1:c.663_667delinsGCTAA ENSP00000461626.1:p.Thr221=
NM_000212.2:c.663_667delinsGCTAA , LRG_481t1:c.663_667delinsGCTAA NP_000203.2:p.Thr221=
NM_000212.3:c.663_667delinsGCTAA MANE Select NP_000203.2:p.Thr221=