Canonical Allele Identifier: CA8622913
Gene: ITGB3 HGNC NCBI

Linked Data

dbSNP Id: rs750801874

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47283518T>A , CM000679.2:g.47283518T>A GRCh38
NC_000017.10:g.45360884T>A , CM000679.1:g.45360884T>A GRCh37
NC_000017.9:g.42715883T>A NCBI36
NG_008332.2:g.34677T>A , LRG_481:g.34677T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.330T>A ENSP00000513002.1:p.Ser110Arg
ENST00000559488.7:c.330T>A MANE Select ENSP00000452786.2:p.Ser110Arg
ENST00000559488.5:c.330T>A ENSP00000452786.1:p.Ser110Arg
ENST00000560629.1:c.295T>A
ENST00000571680.1:c.330T>A ENSP00000461626.1:p.Ser110Arg
NM_000212.2:c.330T>A , LRG_481t1:c.330T>A NP_000203.2:p.Ser110Arg
NM_000212.3:c.330T>A MANE Select NP_000203.2:p.Ser110Arg