Canonical Allele Identifier: CA400023442

Gene: ITGB3

Linked Data

• gnomAD v4: 17-47286296-A-T
• MyVariant Identifiers: chr17:g.45363662A>T (hg19) ; chr17:g.47286296A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47286296A>T , CM000679.2:g.47286296A>T	GRCh38
NC_000017.10:g.45363662A>T , CM000679.1:g.45363662A>T	GRCh37
NC_000017.9:g.42718661A>T	NCBI36
NG_008332.2:g.37455A>T , LRG_481:g.37455A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696963.1:c.651A>T	ENSP00000513002.1:p.Lys217Asn
ENST00000559488.7:c.651A>T MANE Select	ENSP00000452786.2:p.Lys217Asn
ENST00000559488.5:c.651A>T	ENSP00000452786.1:p.Lys217Asn
ENST00000560629.1:c.616A>T
ENST00000571680.1:c.651A>T	ENSP00000461626.1:p.Lys217Asn
NM_000212.2:c.651A>T , LRG_481t1:c.651A>T	NP_000203.2:p.Lys217Asn
NM_000212.3:c.651A>T MANE Select	NP_000203.2:p.Lys217Asn