Canonical Allele Identifier: CA400023259

Gene: ITGB3

Linked Data

• MyVariant Identifiers: chr17:g.45362024A>T (hg19) ; chr17:g.47284658A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47284658A>T , CM000679.2:g.47284658A>T	GRCh38
NC_000017.10:g.45362024A>T , CM000679.1:g.45362024A>T	GRCh37
NC_000017.9:g.42717023A>T	NCBI36
NG_008332.2:g.35817A>T , LRG_481:g.35817A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696963.1:c.577A>T	ENSP00000513002.1:p.Ile193Phe
ENST00000559488.7:c.577A>T MANE Select	ENSP00000452786.2:p.Ile193Phe
ENST00000559488.5:c.577A>T	ENSP00000452786.1:p.Ile193Phe
ENST00000560629.1:c.542A>T
ENST00000571680.1:c.577A>T	ENSP00000461626.1:p.Ile193Phe
NM_000212.2:c.577A>T , LRG_481t1:c.577A>T	NP_000203.2:p.Ile193Phe
NM_000212.3:c.577A>T MANE Select	NP_000203.2:p.Ile193Phe