Canonical Allele Identifier: CA2262606034
Gene: ITGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47286422T= , CM000679.2:g.47286422T= GRCh38
NC_000017.10:g.45363788T= , CM000679.1:g.45363788T= GRCh37
NC_000017.9:g.42718787T= NCBI36
NG_008332.2:g.37581T= , LRG_481:g.37581T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.777T= ENSP00000513002.1:p.Asp259=
ENST00000559488.7:c.777T= MANE Select ENSP00000452786.2:p.Asp259=
ENST00000559488.5:c.777T= ENSP00000452786.1:p.Asp259=
ENST00000560629.1:c.742T=
ENST00000571680.1:c.777T= ENSP00000461626.1:p.Asp259=
NM_000212.2:c.777T= , LRG_481t1:c.777T= NP_000203.2:p.Asp259=
NM_000212.3:c.777T= MANE Select NP_000203.2:p.Asp259=