Canonical Allele Identifier: CA8622889
Gene: ITGB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 697901
dbSNP Id: rs373101628

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47283368C>T , CM000679.2:g.47283368C>T GRCh38
NC_000017.10:g.45360734C>T , CM000679.1:g.45360734C>T GRCh37
NC_000017.9:g.42715733C>T NCBI36
NG_008332.2:g.34527C>T , LRG_481:g.34527C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.180C>T ENSP00000513002.1:p.Gly60=
ENST00000559488.7:c.180C>T MANE Select ENSP00000452786.2:p.Gly60=
ENST00000559488.5:c.180C>T ENSP00000452786.1:p.Gly60=
ENST00000560629.1:c.145C>T
ENST00000571680.1:c.180C>T ENSP00000461626.1:p.Gly60=
NM_000212.2:c.180C>T , LRG_481t1:c.180C>T NP_000203.2:p.Gly60=
NM_000212.3:c.180C>T MANE Select NP_000203.2:p.Gly60=