Canonical Allele Identifier: CA772537311
Gene: ITGB3 HGNC NCBI

Linked Data

dbSNP Id: rs1485345876
gnomAD v3: 17-47286522-A-G
gnomAD v4: 17-47286522-A-G
MyVariant Identifiers: chr17:g.45363888A>G (hg19) chr17:g.47286522A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47286522A>G , CM000679.2:g.47286522A>G GRCh38
NC_000017.10:g.45363888A>G , CM000679.1:g.45363888A>G GRCh37
NC_000017.9:g.42718887A>G NCBI36
NG_008332.2:g.37681A>G , LRG_481:g.37681A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.777+100A>G ENSP00000513002.1:n.777+100A>G
ENST00000559488.7:c.777+100A>G MANE Select ENSP00000452786.2:n.777+100A>G
ENST00000559488.5:c.777+100A>G ENSP00000452786.1:n.777+100A>G
ENST00000560629.1:c.742+100A>G
ENST00000571680.1:c.777+100A>G ENSP00000461626.1:n.777+100A>G
NM_000212.2:c.777+100A>G , LRG_481t1:c.777+100A>G NP_000203.2:n.777+100A>G
NM_000212.3:c.777+100A>G MANE Select NP_000203.2:n.777+100A>G
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