Canonical Allele Identifier: CA400023316
Gene: ITGB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2984069
ClinVar RCV Id: RCV003843228
dbSNP Id: rs1216762390
MyVariant Identifiers: chr17:g.45362050C>A (hg19) chr17:g.47284684C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47284684C>A , CM000679.2:g.47284684C>A GRCh38
NC_000017.10:g.45362050C>A , CM000679.1:g.45362050C>A GRCh37
NC_000017.9:g.42717049C>A NCBI36
NG_008332.2:g.35843C>A , LRG_481:g.35843C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.603C>A ENSP00000513002.1:p.Asn201Lys
ENST00000559488.7:c.603C>A MANE Select ENSP00000452786.2:p.Asn201Lys
ENST00000559488.5:c.603C>A ENSP00000452786.1:p.Asn201Lys
ENST00000560629.1:c.568C>A
ENST00000571680.1:c.603C>A ENSP00000461626.1:p.Asn201Lys
NM_000212.2:c.603C>A , LRG_481t1:c.603C>A NP_000203.2:p.Asn201Lys
NM_000212.3:c.603C>A MANE Select NP_000203.2:p.Asn201Lys
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