Canonical Allele Identifier: CA400020592
Gene: ITGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47283420G>A , CM000679.2:g.47283420G>A GRCh38
NC_000017.10:g.45360786G>A , CM000679.1:g.45360786G>A GRCh37
NC_000017.9:g.42715785G>A NCBI36
NG_008332.2:g.34579G>A , LRG_481:g.34579G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.232G>A ENSP00000513002.1:p.Glu78Lys
ENST00000559488.7:c.232G>A MANE Select ENSP00000452786.2:p.Glu78Lys
ENST00000559488.5:c.232G>A ENSP00000452786.1:p.Glu78Lys
ENST00000560629.1:c.197G>A
ENST00000571680.1:c.232G>A ENSP00000461626.1:p.Glu78Lys
NM_000212.2:c.232G>A , LRG_481t1:c.232G>A NP_000203.2:p.Glu78Lys
NM_000212.3:c.232G>A MANE Select NP_000203.2:p.Glu78Lys