Canonical Allele Identifier: CA2262606048
Gene: ITGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47286453T= , CM000679.2:g.47286453T= GRCh38
NC_000017.10:g.45363819T= , CM000679.1:g.45363819T= GRCh37
NC_000017.9:g.42718818T= NCBI36
NG_008332.2:g.37612T= , LRG_481:g.37612T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.777+31T= ENSP00000513002.1:n.777+31T=
ENST00000559488.7:c.777+31T= MANE Select ENSP00000452786.2:n.777+31T=
ENST00000559488.5:c.777+31T= ENSP00000452786.1:n.777+31T=
ENST00000560629.1:c.742+31T=
ENST00000571680.1:c.777+31T= ENSP00000461626.1:n.777+31T=
NM_000212.2:c.777+31T= , LRG_481t1:c.777+31T= NP_000203.2:n.777+31T=
NM_000212.3:c.777+31T= MANE Select NP_000203.2:n.777+31T=