Canonical Allele Identifier: CA400023558
Gene: ITGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47286351C>G , CM000679.2:g.47286351C>G GRCh38
NC_000017.10:g.45363717C>G , CM000679.1:g.45363717C>G GRCh37
NC_000017.9:g.42718716C>G NCBI36
NG_008332.2:g.37510C>G , LRG_481:g.37510C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.706C>G ENSP00000513002.1:p.Gln236Glu
ENST00000559488.7:c.706C>G MANE Select ENSP00000452786.2:p.Gln236Glu
ENST00000559488.5:c.706C>G ENSP00000452786.1:p.Gln236Glu
ENST00000560629.1:c.671C>G
ENST00000571680.1:c.706C>G ENSP00000461626.1:p.Gln236Glu
NM_000212.2:c.706C>G , LRG_481t1:c.706C>G NP_000203.2:p.Gln236Glu
NM_000212.3:c.706C>G MANE Select NP_000203.2:p.Gln236Glu