Canonical Allele Identifier: CA291227762
Community Standard Title: NM_000212.3(ITGB3):c.1914-139_1914-138insTG
Gene: ITGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47300339_47300340insTG , CM000679.2:g.47300339_47300340insTG GRCh38
NC_000017.10:g.45377705_45377706insTG , CM000679.1:g.45377705_45377706insTG GRCh37
NC_000017.9:g.42732704_42732705insTG NCBI36
NG_008332.2:g.51498_51499insTG , LRG_481:g.51498_51499insTG

Transcript Alleles

HGVS Amino-acid Change
NM_000212.3:c.1914-139_1914-138insTG MANE Select NP_000203.2:n.1914-139_1914-138insTG
ENST00000559488.7:c.1914-139_1914-138insTG MANE Select ENSP00000452786.2:n.1914-139_1914-138insTG
NM_000212.2:c.1914-139_1914-138insTG , LRG_481t1:c.1914-139_1914-138insTG NP_000203.2:n.1914-139_1914-138insTG
ENST00000559488.5:c.1914-139_1914-138insTG ENSP00000452786.1:n.1914-139_1914-138insTG
ENST00000560629.1:c.1879-139_1879-138insTG
ENST00000696963.1:c.1914-139_1914-138insTG ENSP00000513002.1:n.1914-139_1914-138insTG