Canonical Allele Identifier: CA400023545
Gene: ITGB3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.45363712A>C (hg19) chr17:g.47286346A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47286346A>C , CM000679.2:g.47286346A>C GRCh38
NC_000017.10:g.45363712A>C , CM000679.1:g.45363712A>C GRCh37
NC_000017.9:g.42718711A>C NCBI36
NG_008332.2:g.37505A>C , LRG_481:g.37505A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.701A>C ENSP00000513002.1:p.Lys234Thr
ENST00000559488.7:c.701A>C MANE Select ENSP00000452786.2:p.Lys234Thr
ENST00000559488.5:c.701A>C ENSP00000452786.1:p.Lys234Thr
ENST00000560629.1:c.666A>C
ENST00000571680.1:c.701A>C ENSP00000461626.1:p.Lys234Thr
NM_000212.2:c.701A>C , LRG_481t1:c.701A>C NP_000203.2:p.Lys234Thr
NM_000212.3:c.701A>C MANE Select NP_000203.2:p.Lys234Thr
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