Canonical Allele Identifier: CA2262605000
Gene: ITGB3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47283757G= , CM000679.2:g.47283757G= GRCh38
NC_000017.10:g.45361123G= , CM000679.1:g.45361123G= GRCh37
NC_000017.9:g.42716122G= NCBI36
NG_008332.2:g.34916G= , LRG_481:g.34916G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.361+208G= ENSP00000513002.1:n.361+208G=
ENST00000559488.7:c.361+208G= MANE Select ENSP00000452786.2:n.361+208G=
ENST00000559488.5:c.361+208G= ENSP00000452786.1:n.361+208G=
ENST00000560629.1:c.326+208G=
ENST00000571680.1:c.361+208G= ENSP00000461626.1:n.361+208G=
NM_000212.2:c.361+208G= , LRG_481t1:c.361+208G= NP_000203.2:n.361+208G=
NM_000212.3:c.361+208G= MANE Select NP_000203.2:n.361+208G=
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