Canonical Allele Identifier: CA2262604941
Gene: ITGB3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47283630_47283631delinsTG , CM000679.2:g.47283630_47283631delinsTG GRCh38
NC_000017.10:g.45360996_45360997delinsTG , CM000679.1:g.45360996_45360997delinsTG GRCh37
NC_000017.9:g.42715995_42715996delinsTG NCBI36
NG_008332.2:g.34789_34790delinsTG , LRG_481:g.34789_34790delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.361+81_361+82delinsTG ENSP00000513002.1:n.361+81_361+82delinsTG
ENST00000559488.7:c.361+81_361+82delinsTG MANE Select ENSP00000452786.2:n.361+81_361+82delinsTG
ENST00000559488.5:c.361+81_361+82delinsTG ENSP00000452786.1:n.361+81_361+82delinsTG
ENST00000560629.1:c.326+81_326+82delinsTG
ENST00000571680.1:c.361+81_361+82delinsTG ENSP00000461626.1:n.361+81_361+82delinsTG
NM_000212.2:c.361+81_361+82delinsTG , LRG_481t1:c.361+81_361+82delinsTG NP_000203.2:n.361+81_361+82delinsTG
NM_000212.3:c.361+81_361+82delinsTG MANE Select NP_000203.2:n.361+81_361+82delinsTG
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