Canonical Allele Identifier: CA400023508
Gene: ITGB3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.45363697T>A (hg19) chr17:g.47286331T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47286331T>A , CM000679.2:g.47286331T>A GRCh38
NC_000017.10:g.45363697T>A , CM000679.1:g.45363697T>A GRCh37
NC_000017.9:g.42718696T>A NCBI36
NG_008332.2:g.37490T>A , LRG_481:g.37490T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.686T>A ENSP00000513002.1:p.Phe229Tyr
ENST00000559488.7:c.686T>A MANE Select ENSP00000452786.2:p.Phe229Tyr
ENST00000559488.5:c.686T>A ENSP00000452786.1:p.Phe229Tyr
ENST00000560629.1:c.651T>A
ENST00000571680.1:c.686T>A ENSP00000461626.1:p.Phe229Tyr
NM_000212.2:c.686T>A , LRG_481t1:c.686T>A NP_000203.2:p.Phe229Tyr
NM_000212.3:c.686T>A MANE Select NP_000203.2:p.Phe229Tyr
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