Canonical Allele Identifier: CA2262604975
Gene: ITGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47283716C= , CM000679.2:g.47283716C= GRCh38
NC_000017.10:g.45361082C= , CM000679.1:g.45361082C= GRCh37
NC_000017.9:g.42716081C= NCBI36
NG_008332.2:g.34875C= , LRG_481:g.34875C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.361+167C= ENSP00000513002.1:n.361+167C=
ENST00000559488.7:c.361+167C= MANE Select ENSP00000452786.2:n.361+167C=
ENST00000559488.5:c.361+167C= ENSP00000452786.1:n.361+167C=
ENST00000560629.1:c.326+167C=
ENST00000571680.1:c.361+167C= ENSP00000461626.1:n.361+167C=
NM_000212.2:c.361+167C= , LRG_481t1:c.361+167C= NP_000203.2:n.361+167C=
NM_000212.3:c.361+167C= MANE Select NP_000203.2:n.361+167C=