Canonical Allele Identifier: CA400023289

Gene: ITGB3

Linked Data

• MyVariant Identifiers: chr17:g.45362038G>T (hg19) ; chr17:g.47284672G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47284672G>T , CM000679.2:g.47284672G>T	GRCh38
NC_000017.10:g.45362038G>T , CM000679.1:g.45362038G>T	GRCh37
NC_000017.9:g.42717037G>T	NCBI36
NG_008332.2:g.35831G>T , LRG_481:g.35831G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696963.1:c.591G>T	ENSP00000513002.1:p.Glu197Asp
ENST00000559488.7:c.591G>T MANE Select	ENSP00000452786.2:p.Glu197Asp
ENST00000559488.5:c.591G>T	ENSP00000452786.1:p.Glu197Asp
ENST00000560629.1:c.556G>T
ENST00000571680.1:c.591G>T	ENSP00000461626.1:p.Glu197Asp
NM_000212.2:c.591G>T , LRG_481t1:c.591G>T	NP_000203.2:p.Glu197Asp
NM_000212.3:c.591G>T MANE Select	NP_000203.2:p.Glu197Asp