Canonical Allele Identifier: CA500431999

Gene: ITGB3

Linked Data

• MyVariant Identifiers: chr17:g.45363707A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47286341A>G , CM000679.2:g.47286341A>G	GRCh38
NC_000017.10:g.45363707A>G , CM000679.1:g.45363707A>G	GRCh37
NC_000017.9:g.42718706A>G	NCBI36
NG_008332.2:g.37500A>G , LRG_481:g.37500A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696963.1:c.696A>G	ENSP00000513002.1:p.Glu232=
ENST00000559488.7:c.696A>G MANE Select	ENSP00000452786.2:p.Glu232=
ENST00000559488.5:c.696A>G	ENSP00000452786.1:p.Glu232=
ENST00000560629.1:c.661A>G
ENST00000571680.1:c.696A>G	ENSP00000461626.1:p.Glu232=
NM_000212.2:c.696A>G , LRG_481t1:c.696A>G	NP_000203.2:p.Glu232=
NM_000212.3:c.696A>G MANE Select	NP_000203.2:p.Glu232=