Canonical Allele Identifier: CA400023124
Gene: ITGB3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.45361992T>A (hg19) chr17:g.47284626T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47284626T>A , CM000679.2:g.47284626T>A GRCh38
NC_000017.10:g.45361992T>A , CM000679.1:g.45361992T>A GRCh37
NC_000017.9:g.42716991T>A NCBI36
NG_008332.2:g.35785T>A , LRG_481:g.35785T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.545T>A ENSP00000513002.1:p.Phe182Tyr
ENST00000559488.7:c.545T>A MANE Select ENSP00000452786.2:p.Phe182Tyr
ENST00000559488.5:c.545T>A ENSP00000452786.1:p.Phe182Tyr
ENST00000560629.1:c.510T>A
ENST00000571680.1:c.545T>A ENSP00000461626.1:p.Phe182Tyr
NM_000212.2:c.545T>A , LRG_481t1:c.545T>A NP_000203.2:p.Phe182Tyr
NM_000212.3:c.545T>A MANE Select NP_000203.2:p.Phe182Tyr
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