Canonical Allele Identifier: CA8622946
Gene: ITGB3 HGNC NCBI

Linked Data

dbSNP Id: rs745721126
ExAC: 17:45361806 C / G
gnomAD v2: 17-45361806-C-G
gnomAD v4: 17-47284440-C-G
MyVariant Identifiers: chr17:g.45361806C>G (hg19) chr17:g.47284440C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47284440C>G , CM000679.2:g.47284440C>G GRCh38
NC_000017.10:g.45361806C>G , CM000679.1:g.45361806C>G GRCh37
NC_000017.9:g.42716805C>G NCBI36
NG_008332.2:g.35599C>G , LRG_481:g.35599C>G

Transcript Alleles

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