Canonical Allele Identifier: CA400023251
Gene: ITGB3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.45362021T>C (hg19) chr17:g.47284655T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47284655T>C , CM000679.2:g.47284655T>C GRCh38
NC_000017.10:g.45362021T>C , CM000679.1:g.45362021T>C GRCh37
NC_000017.9:g.42717020T>C NCBI36
NG_008332.2:g.35814T>C , LRG_481:g.35814T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.574T>C ENSP00000513002.1:p.Tyr192His
ENST00000559488.7:c.574T>C MANE Select ENSP00000452786.2:p.Tyr192His
ENST00000559488.5:c.574T>C ENSP00000452786.1:p.Tyr192His
ENST00000560629.1:c.539T>C
ENST00000571680.1:c.574T>C ENSP00000461626.1:p.Tyr192His
NM_000212.2:c.574T>C , LRG_481t1:c.574T>C NP_000203.2:p.Tyr192His
NM_000212.3:c.574T>C MANE Select NP_000203.2:p.Tyr192His
Search 100 bp 5'
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