Canonical Allele Identifier: CA400020565
Gene: ITGB3 HGNC NCBI

Linked Data

dbSNP Id: rs2065090967

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47283408A>G , CM000679.2:g.47283408A>G GRCh38
NC_000017.10:g.45360774A>G , CM000679.1:g.45360774A>G GRCh37
NC_000017.9:g.42715773A>G NCBI36
NG_008332.2:g.34567A>G , LRG_481:g.34567A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.220A>G ENSP00000513002.1:p.Asn74Asp
ENST00000559488.7:c.220A>G MANE Select ENSP00000452786.2:p.Asn74Asp
ENST00000559488.5:c.220A>G ENSP00000452786.1:p.Asn74Asp
ENST00000560629.1:c.185A>G
ENST00000571680.1:c.220A>G ENSP00000461626.1:p.Asn74Asp
NM_000212.2:c.220A>G , LRG_481t1:c.220A>G NP_000203.2:p.Asn74Asp
NM_000212.3:c.220A>G MANE Select NP_000203.2:p.Asn74Asp