Canonical Allele Identifier: CA8622941
Gene: ITGB3 HGNC NCBI

Linked Data

dbSNP Id: rs750191294

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47284413_47284415del , CM000679.2:g.47284413_47284415del GRCh38
NC_000017.10:g.45361779_45361781del , CM000679.1:g.45361779_45361781del GRCh37
NC_000017.9:g.42716778_42716780del NCBI36
NG_008332.2:g.35572_35574del , LRG_481:g.35572_35574del

Transcript Alleles

HGVS Amino-acid change
ENST00000696963.1:c.362-30_362-28del ENSP00000513002.1:n.362-30_362-28del
ENST00000559488.7:c.362-30_362-28del MANE Select ENSP00000452786.2:n.362-30_362-28del
ENST00000559488.5:c.362-30_362-28del ENSP00000452786.1:n.362-30_362-28del
ENST00000560629.1:c.327-30_327-28del
ENST00000571680.1:c.362-30_362-28del ENSP00000461626.1:n.362-30_362-28del
NM_000212.2:c.362-30_362-28del , LRG_481t1:c.362-30_362-28del NP_000203.2:n.362-30_362-28del
NM_000212.3:c.362-30_362-28del MANE Select NP_000203.2:n.362-30_362-28del