Canonical Allele Identifier: CA400023551
Gene: ITGB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2432923
ClinVar RCV Id: RCV003131283
MyVariant Identifiers: chr17:g.45363714A>G (hg19) chr17:g.47286348A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47286348A>G , CM000679.2:g.47286348A>G GRCh38
NC_000017.10:g.45363714A>G , CM000679.1:g.45363714A>G GRCh37
NC_000017.9:g.42718713A>G NCBI36
NG_008332.2:g.37507A>G , LRG_481:g.37507A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.703A>G ENSP00000513002.1:p.Lys235Glu
ENST00000559488.7:c.703A>G MANE Select ENSP00000452786.2:p.Lys235Glu
ENST00000559488.5:c.703A>G ENSP00000452786.1:p.Lys235Glu
ENST00000560629.1:c.668A>G
ENST00000571680.1:c.703A>G ENSP00000461626.1:p.Lys235Glu
NM_000212.2:c.703A>G , LRG_481t1:c.703A>G NP_000203.2:p.Lys235Glu
NM_000212.3:c.703A>G MANE Select NP_000203.2:p.Lys235Glu
Search 100 bp 5'
Search 100 bp 3'