Canonical Allele Identifier: CA772535687

Gene: ITGB3

Linked Data

• dbSNP Id: rs1294199964
• MyVariant Identifiers: chr17:g.45361181G>T (hg19) ; chr17:g.47283815G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47283815G>T , CM000679.2:g.47283815G>T	GRCh38
NC_000017.10:g.45361181G>T , CM000679.1:g.45361181G>T	GRCh37
NC_000017.9:g.42716180G>T	NCBI36
NG_008332.2:g.34974G>T , LRG_481:g.34974G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696963.1:c.361+266G>T	ENSP00000513002.1:n.361+266G>T
ENST00000559488.7:c.361+266G>T MANE Select	ENSP00000452786.2:n.361+266G>T
ENST00000559488.5:c.361+266G>T	ENSP00000452786.1:n.361+266G>T
ENST00000560629.1:c.326+266G>T
ENST00000571680.1:c.361+266G>T	ENSP00000461626.1:n.361+266G>T
NM_000212.2:c.361+266G>T , LRG_481t1:c.361+266G>T	NP_000203.2:n.361+266G>T
NM_000212.3:c.361+266G>T MANE Select	NP_000203.2:n.361+266G>T