Canonical Allele Identifier: CA400023461
Gene: ITGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47286306A>C , CM000679.2:g.47286306A>C GRCh38
NC_000017.10:g.45363672A>C , CM000679.1:g.45363672A>C GRCh37
NC_000017.9:g.42718671A>C NCBI36
NG_008332.2:g.37465A>C , LRG_481:g.37465A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.661A>C ENSP00000513002.1:p.Thr221Pro
ENST00000559488.7:c.661A>C MANE Select ENSP00000452786.2:p.Thr221Pro
ENST00000559488.5:c.661A>C ENSP00000452786.1:p.Thr221Pro
ENST00000560629.1:c.626A>C
ENST00000571680.1:c.661A>C ENSP00000461626.1:p.Thr221Pro
NM_000212.2:c.661A>C , LRG_481t1:c.661A>C NP_000203.2:p.Thr221Pro
NM_000212.3:c.661A>C MANE Select NP_000203.2:p.Thr221Pro