Canonical Allele Identifier: CA2262604852
Gene: ITGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47283415C= , CM000679.2:g.47283415C= GRCh38
NC_000017.10:g.45360781C= , CM000679.1:g.45360781C= GRCh37
NC_000017.9:g.42715780C= NCBI36
NG_008332.2:g.34574C= , LRG_481:g.34574C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.227C= ENSP00000513002.1:p.Ala76=
ENST00000559488.7:c.227C= MANE Select ENSP00000452786.2:p.Ala76=
ENST00000559488.5:c.227C= ENSP00000452786.1:p.Ala76=
ENST00000560629.1:c.192C=
ENST00000571680.1:c.227C= ENSP00000461626.1:p.Ala76=
NM_000212.2:c.227C= , LRG_481t1:c.227C= NP_000203.2:p.Ala76=
NM_000212.3:c.227C= MANE Select NP_000203.2:p.Ala76=