Canonical Allele Identifier: CA772535224
Gene: ITGB3 HGNC NCBI

Linked Data

dbSNP Id: rs1277924658

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47283295A>T , CM000679.2:g.47283295A>T GRCh38
NC_000017.10:g.45360661A>T , CM000679.1:g.45360661A>T GRCh37
NC_000017.9:g.42715660A>T NCBI36
NG_008332.2:g.34454A>T , LRG_481:g.34454A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696963.1:c.166-59A>T ENSP00000513002.1:n.166-59A>T
ENST00000559488.7:c.166-59A>T MANE Select ENSP00000452786.2:n.166-59A>T
ENST00000559488.5:c.166-59A>T ENSP00000452786.1:n.166-59A>T
ENST00000560629.1:c.131-59A>T
ENST00000571680.1:c.166-59A>T ENSP00000461626.1:n.166-59A>T
NM_000212.2:c.166-59A>T , LRG_481t1:c.166-59A>T NP_000203.2:n.166-59A>T
NM_000212.3:c.166-59A>T MANE Select NP_000203.2:n.166-59A>T