Canonical Allele Identifier: CA400023455
Gene: ITGB3 HGNC NCBI

Linked Data

dbSNP Id: rs1311161158

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47286301T>C , CM000679.2:g.47286301T>C GRCh38
NC_000017.10:g.45363667T>C , CM000679.1:g.45363667T>C GRCh37
NC_000017.9:g.42718666T>C NCBI36
NG_008332.2:g.37460T>C , LRG_481:g.37460T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.656T>C ENSP00000513002.1:p.Val219Ala
ENST00000559488.7:c.656T>C MANE Select ENSP00000452786.2:p.Val219Ala
ENST00000559488.5:c.656T>C ENSP00000452786.1:p.Val219Ala
ENST00000560629.1:c.621T>C
ENST00000571680.1:c.656T>C ENSP00000461626.1:p.Val219Ala
NM_000212.2:c.656T>C , LRG_481t1:c.656T>C NP_000203.2:p.Val219Ala
NM_000212.3:c.656T>C MANE Select NP_000203.2:p.Val219Ala