Canonical Allele Identifier: CA400023692
Gene: ITGB3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.45363778C>T (hg19) chr17:g.47286412C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47286412C>T , CM000679.2:g.47286412C>T GRCh38
NC_000017.10:g.45363778C>T , CM000679.1:g.45363778C>T GRCh37
NC_000017.9:g.42718777C>T NCBI36
NG_008332.2:g.37571C>T , LRG_481:g.37571C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.767C>T ENSP00000513002.1:p.Thr256Ile
ENST00000559488.7:c.767C>T MANE Select ENSP00000452786.2:p.Thr256Ile
ENST00000559488.5:c.767C>T ENSP00000452786.1:p.Thr256Ile
ENST00000560629.1:c.732C>T
ENST00000571680.1:c.767C>T ENSP00000461626.1:p.Thr256Ile
NM_000212.2:c.767C>T , LRG_481t1:c.767C>T NP_000203.2:p.Thr256Ile
NM_000212.3:c.767C>T MANE Select NP_000203.2:p.Thr256Ile
Search 100 bp 5'
Search 100 bp 3'