Canonical Allele Identifier: CA400023622
Gene: ITGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47286382A>C , CM000679.2:g.47286382A>C GRCh38
NC_000017.10:g.45363748A>C , CM000679.1:g.45363748A>C GRCh37
NC_000017.9:g.42718747A>C NCBI36
NG_008332.2:g.37541A>C , LRG_481:g.37541A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.737A>C ENSP00000513002.1:p.Glu246Ala
ENST00000559488.7:c.737A>C MANE Select ENSP00000452786.2:p.Glu246Ala
ENST00000559488.5:c.737A>C ENSP00000452786.1:p.Glu246Ala
ENST00000560629.1:c.702A>C
ENST00000571680.1:c.737A>C ENSP00000461626.1:p.Glu246Ala
NM_000212.2:c.737A>C , LRG_481t1:c.737A>C NP_000203.2:p.Glu246Ala
NM_000212.3:c.737A>C MANE Select NP_000203.2:p.Glu246Ala