Canonical Allele Identifier: CA2262605369
Gene: ITGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47284684C= , CM000679.2:g.47284684C= GRCh38
NC_000017.10:g.45362050C= , CM000679.1:g.45362050C= GRCh37
NC_000017.9:g.42717049C= NCBI36
NG_008332.2:g.35843C= , LRG_481:g.35843C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.603C= ENSP00000513002.1:p.Asn201=
ENST00000559488.7:c.603C= MANE Select ENSP00000452786.2:p.Asn201=
ENST00000559488.5:c.603C= ENSP00000452786.1:p.Asn201=
ENST00000560629.1:c.568C=
ENST00000571680.1:c.603C= ENSP00000461626.1:p.Asn201=
NM_000212.2:c.603C= , LRG_481t1:c.603C= NP_000203.2:p.Asn201=
NM_000212.3:c.603C= MANE Select NP_000203.2:p.Asn201=