Canonical Allele Identifier: CA400020479
Gene: ITGB3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.45360748A>C (hg19) chr17:g.47283382A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47283382A>C , CM000679.2:g.47283382A>C GRCh38
NC_000017.10:g.45360748A>C , CM000679.1:g.45360748A>C GRCh37
NC_000017.9:g.42715747A>C NCBI36
NG_008332.2:g.34541A>C , LRG_481:g.34541A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696963.1:c.194A>C ENSP00000513002.1:p.Asp65Ala
ENST00000559488.7:c.194A>C MANE Select ENSP00000452786.2:p.Asp65Ala
ENST00000559488.5:c.194A>C ENSP00000452786.1:p.Asp65Ala
ENST00000560629.1:c.159A>C
ENST00000571680.1:c.194A>C ENSP00000461626.1:p.Asp65Ala
NM_000212.2:c.194A>C , LRG_481t1:c.194A>C NP_000203.2:p.Asp65Ala
NM_000212.3:c.194A>C MANE Select NP_000203.2:p.Asp65Ala
Search 100 bp 5'
Search 100 bp 3'