Canonical Allele Identifier: CA400021968
Gene: ITGB3 HGNC NCBI

Linked Data

dbSNP Id: rs2065095681

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47284520T>C , CM000679.2:g.47284520T>C GRCh38
NC_000017.10:g.45361886T>C , CM000679.1:g.45361886T>C GRCh37
NC_000017.9:g.42716885T>C NCBI36
NG_008332.2:g.35679T>C , LRG_481:g.35679T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.439T>C ENSP00000513002.1:p.Ser147Pro
ENST00000559488.7:c.439T>C MANE Select ENSP00000452786.2:p.Ser147Pro
ENST00000559488.5:c.439T>C ENSP00000452786.1:p.Ser147Pro
ENST00000560629.1:c.404T>C
ENST00000571680.1:c.439T>C ENSP00000461626.1:p.Ser147Pro
NM_000212.2:c.439T>C , LRG_481t1:c.439T>C NP_000203.2:p.Ser147Pro
NM_000212.3:c.439T>C MANE Select NP_000203.2:p.Ser147Pro