Canonical Allele Identifier: CA500432040
Gene: ITGB3 HGNC NCBI

Linked Data

dbSNP Id: rs2065102874
MyVariant Identifiers: chr17:g.45363767C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47286401C>T , CM000679.2:g.47286401C>T GRCh38
NC_000017.10:g.45363767C>T , CM000679.1:g.45363767C>T GRCh37
NC_000017.9:g.42718766C>T NCBI36
NG_008332.2:g.37560C>T , LRG_481:g.37560C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696963.1:c.756C>T ENSP00000513002.1:p.Ile252=
ENST00000559488.7:c.756C>T MANE Select ENSP00000452786.2:p.Ile252=
ENST00000559488.5:c.756C>T ENSP00000452786.1:p.Ile252=
ENST00000560629.1:c.721C>T
ENST00000571680.1:c.756C>T ENSP00000461626.1:p.Ile252=
NM_000212.2:c.756C>T , LRG_481t1:c.756C>T NP_000203.2:p.Ile252=
NM_000212.3:c.756C>T MANE Select NP_000203.2:p.Ile252=
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