Canonical Allele Identifier: CA2262604929
Gene: ITGB3 HGNC NCBI

Linked Data

dbSNP Id: rs2065091995

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47283609_47283614del , CM000679.2:g.47283609_47283614del GRCh38
NC_000017.10:g.45360975_45360980del , CM000679.1:g.45360975_45360980del GRCh37
NC_000017.9:g.42715974_42715979del NCBI36
NG_008332.2:g.34768_34773del , LRG_481:g.34768_34773del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.361+60_361+65del ENSP00000513002.1:n.361+60_361+65del
ENST00000559488.7:c.361+60_361+65del MANE Select ENSP00000452786.2:n.361+60_361+65del
ENST00000559488.5:c.361+60_361+65del ENSP00000452786.1:n.361+60_361+65del
ENST00000560629.1:c.326+60_326+65del
ENST00000571680.1:c.361+60_361+65del ENSP00000461626.1:n.361+60_361+65del
NM_000212.2:c.361+60_361+65del , LRG_481t1:c.361+60_361+65del NP_000203.2:n.361+60_361+65del
NM_000212.3:c.361+60_361+65del MANE Select NP_000203.2:n.361+60_361+65del