Canonical Allele Identifier: CA8623034
Gene: ITGB3 HGNC NCBI

Linked Data

dbSNP Id: rs771080439
ExAC: 17:45363777 A / G
gnomAD v2: 17-45363777-A-G
MyVariant Identifiers: chr17:g.45363777A>G (hg19) chr17:g.47286411A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47286411A>G , CM000679.2:g.47286411A>G GRCh38
NC_000017.10:g.45363777A>G , CM000679.1:g.45363777A>G GRCh37
NC_000017.9:g.42718776A>G NCBI36
NG_008332.2:g.37570A>G , LRG_481:g.37570A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.766A>G ENSP00000513002.1:p.Thr256Ala
ENST00000559488.7:c.766A>G MANE Select ENSP00000452786.2:p.Thr256Ala
ENST00000559488.5:c.766A>G ENSP00000452786.1:p.Thr256Ala
ENST00000560629.1:c.731A>G
ENST00000571680.1:c.766A>G ENSP00000461626.1:p.Thr256Ala
NM_000212.2:c.766A>G , LRG_481t1:c.766A>G NP_000203.2:p.Thr256Ala
NM_000212.3:c.766A>G MANE Select NP_000203.2:p.Thr256Ala
Search 100 bp 5'
Search 100 bp 3'