Canonical Allele Identifier: CA400020706
Gene: ITGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47283451G>C , CM000679.2:g.47283451G>C GRCh38
NC_000017.10:g.45360817G>C , CM000679.1:g.45360817G>C GRCh37
NC_000017.9:g.42715816G>C NCBI36
NG_008332.2:g.34610G>C , LRG_481:g.34610G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.263G>C ENSP00000513002.1:p.Arg88Pro
ENST00000559488.7:c.263G>C MANE Select ENSP00000452786.2:p.Arg88Pro
ENST00000559488.5:c.263G>C ENSP00000452786.1:p.Arg88Pro
ENST00000560629.1:c.228G>C
ENST00000571680.1:c.263G>C ENSP00000461626.1:p.Arg88Pro
NM_000212.2:c.263G>C , LRG_481t1:c.263G>C NP_000203.2:p.Arg88Pro
NM_000212.3:c.263G>C MANE Select NP_000203.2:p.Arg88Pro