Canonical Allele Identifier: CA400023238
Gene: ITGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47284650A>T , CM000679.2:g.47284650A>T GRCh38
NC_000017.10:g.45362016A>T , CM000679.1:g.45362016A>T GRCh37
NC_000017.9:g.42717015A>T NCBI36
NG_008332.2:g.35809A>T , LRG_481:g.35809A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.569A>T ENSP00000513002.1:p.Tyr190Phe
ENST00000559488.7:c.569A>T MANE Select ENSP00000452786.2:p.Tyr190Phe
ENST00000559488.5:c.569A>T ENSP00000452786.1:p.Tyr190Phe
ENST00000560629.1:c.534A>T
ENST00000571680.1:c.569A>T ENSP00000461626.1:p.Tyr190Phe
NM_000212.2:c.569A>T , LRG_481t1:c.569A>T NP_000203.2:p.Tyr190Phe
NM_000212.3:c.569A>T MANE Select NP_000203.2:p.Tyr190Phe