Canonical Allele Identifier: CA2262606032
Gene: ITGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47286416_47286418delinsCTG , CM000679.2:g.47286416_47286418delinsCTG GRCh38
NC_000017.10:g.45363782_45363784delinsCTG , CM000679.1:g.45363782_45363784delinsCTG GRCh37
NC_000017.9:g.42718781_42718783delinsCTG NCBI36
NG_008332.2:g.37575_37577delinsCTG , LRG_481:g.37575_37577delinsCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.771_773delinsCTG ENSP00000513002.1:p.Val257=
ENST00000559488.7:c.771_773delinsCTG MANE Select ENSP00000452786.2:p.Val257=
ENST00000559488.5:c.771_773delinsCTG ENSP00000452786.1:p.Val257=
ENST00000560629.1:c.736_738delinsCTG
ENST00000571680.1:c.771_773delinsCTG ENSP00000461626.1:p.Val257=
NM_000212.2:c.771_773delinsCTG , LRG_481t1:c.771_773delinsCTG NP_000203.2:p.Val257=
NM_000212.3:c.771_773delinsCTG MANE Select NP_000203.2:p.Val257=