Canonical Allele Identifier: CA2638435567
Gene: ITGB3 HGNC NCBI

Linked Data

gnomAD v4: 17-47286540-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47286540C>A , CM000679.2:g.47286540C>A GRCh38
NC_000017.10:g.45363906C>A , CM000679.1:g.45363906C>A GRCh37
NC_000017.9:g.42718905C>A NCBI36
NG_008332.2:g.37699C>A , LRG_481:g.37699C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.777+118C>A ENSP00000513002.1:n.777+118C>A
ENST00000559488.7:c.777+118C>A MANE Select ENSP00000452786.2:n.777+118C>A
ENST00000559488.5:c.777+118C>A ENSP00000452786.1:n.777+118C>A
ENST00000560629.1:c.742+118C>A
ENST00000571680.1:c.777+118C>A ENSP00000461626.1:n.777+118C>A
NM_000212.2:c.777+118C>A , LRG_481t1:c.777+118C>A NP_000203.2:n.777+118C>A
NM_000212.3:c.777+118C>A MANE Select NP_000203.2:n.777+118C>A
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