Canonical Allele Identifier: CA626378300

Gene: ITGB3

Linked Data

• dbSNP Id: rs1240648844
• gnomAD v2: 17-45361786-A-G
• gnomAD v4: 17-47284420-A-G
• MyVariant Identifiers: chr17:g.45361786A>G (hg19) ; chr17:g.47284420A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47284420A>G , CM000679.2:g.47284420A>G	GRCh38
NC_000017.10:g.45361786A>G , CM000679.1:g.45361786A>G	GRCh37
NC_000017.9:g.42716785A>G	NCBI36
NG_008332.2:g.35579A>G , LRG_481:g.35579A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000696963.1:c.362-23A>G	ENSP00000513002.1:n.362-23A>G
ENST00000559488.7:c.362-23A>G MANE Select	ENSP00000452786.2:n.362-23A>G
ENST00000559488.5:c.362-23A>G	ENSP00000452786.1:n.362-23A>G
ENST00000560629.1:c.327-23A>G
ENST00000571680.1:c.362-23A>G	ENSP00000461626.1:n.362-23A>G
NM_000212.2:c.362-23A>G , LRG_481t1:c.362-23A>G	NP_000203.2:n.362-23A>G
NM_000212.3:c.362-23A>G MANE Select	NP_000203.2:n.362-23A>G