Canonical Allele Identifier: CA123256
Gene: ITGB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 13569
dbSNP Id: rs79560904

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47286385G>A , CM000679.2:g.47286385G>A GRCh38
NC_000017.10:g.45363751G>A , CM000679.1:g.45363751G>A GRCh37
NC_000017.9:g.42718750G>A NCBI36
NG_008332.2:g.37544G>A , LRG_481:g.37544G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.740G>A ENSP00000513002.1:p.Gly247Asp
ENST00000559488.7:c.740G>A MANE Select ENSP00000452786.2:p.Gly247Asp
ENST00000559488.5:c.740G>A ENSP00000452786.1:p.Gly247Asp
ENST00000560629.1:c.705G>A
ENST00000571680.1:c.740G>A ENSP00000461626.1:p.Gly247Asp
NM_000212.2:c.740G>A , LRG_481t1:c.740G>A NP_000203.2:p.Gly247Asp
NM_000212.3:c.740G>A MANE Select NP_000203.2:p.Gly247Asp