Canonical Allele Identifier: CA2262606031
Gene: ITGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47286414G= , CM000679.2:g.47286414G= GRCh38
NC_000017.10:g.45363780G= , CM000679.1:g.45363780G= GRCh37
NC_000017.9:g.42718779G= NCBI36
NG_008332.2:g.37573G= , LRG_481:g.37573G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.769G= ENSP00000513002.1:p.Val257=
ENST00000559488.7:c.769G= MANE Select ENSP00000452786.2:p.Val257=
ENST00000559488.5:c.769G= ENSP00000452786.1:p.Val257=
ENST00000560629.1:c.734G=
ENST00000571680.1:c.769G= ENSP00000461626.1:p.Val257=
NM_000212.2:c.769G= , LRG_481t1:c.769G= NP_000203.2:p.Val257=
NM_000212.3:c.769G= MANE Select NP_000203.2:p.Val257=