Canonical Allele Identifier: CA400023557
Gene: ITGB3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.45363717C>A (hg19) chr17:g.47286351C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47286351C>A , CM000679.2:g.47286351C>A GRCh38
NC_000017.10:g.45363717C>A , CM000679.1:g.45363717C>A GRCh37
NC_000017.9:g.42718716C>A NCBI36
NG_008332.2:g.37510C>A , LRG_481:g.37510C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.706C>A ENSP00000513002.1:p.Gln236Lys
ENST00000559488.7:c.706C>A MANE Select ENSP00000452786.2:p.Gln236Lys
ENST00000559488.5:c.706C>A ENSP00000452786.1:p.Gln236Lys
ENST00000560629.1:c.671C>A
ENST00000571680.1:c.706C>A ENSP00000461626.1:p.Gln236Lys
NM_000212.2:c.706C>A , LRG_481t1:c.706C>A NP_000203.2:p.Gln236Lys
NM_000212.3:c.706C>A MANE Select NP_000203.2:p.Gln236Lys
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