Canonical Allele Identifier: CA2501367792
Gene: ITGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47283637_47283640del , CM000679.2:g.47283637_47283640del GRCh38
NC_000017.10:g.45361003_45361006del , CM000679.1:g.45361003_45361006del GRCh37
NC_000017.9:g.42716002_42716005del NCBI36
NG_008332.2:g.34796_34799del , LRG_481:g.34796_34799del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.361+88_361+91del ENSP00000513002.1:n.361+88_361+91del
ENST00000559488.7:c.361+88_361+91del MANE Select ENSP00000452786.2:n.361+88_361+91del
ENST00000559488.5:c.361+88_361+91del ENSP00000452786.1:n.361+88_361+91del
ENST00000560629.1:c.326+88_326+91del
ENST00000571680.1:c.361+88_361+91del ENSP00000461626.1:n.361+88_361+91del
NM_000212.2:c.361+88_361+91del , LRG_481t1:c.361+88_361+91del NP_000203.2:n.361+88_361+91del
NM_000212.3:c.361+88_361+91del MANE Select NP_000203.2:n.361+88_361+91del