Canonical Allele Identifier: CA2638435579
Gene: ITGB3 HGNC NCBI

Linked Data

gnomAD v4: 17-47286554-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47286554A>C , CM000679.2:g.47286554A>C GRCh38
NC_000017.10:g.45363920A>C , CM000679.1:g.45363920A>C GRCh37
NC_000017.9:g.42718919A>C NCBI36
NG_008332.2:g.37713A>C , LRG_481:g.37713A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.777+132A>C ENSP00000513002.1:n.777+132A>C
ENST00000559488.7:c.777+132A>C MANE Select ENSP00000452786.2:n.777+132A>C
ENST00000559488.5:c.777+132A>C ENSP00000452786.1:n.777+132A>C
ENST00000560629.1:c.742+132A>C
ENST00000571680.1:c.777+132A>C ENSP00000461626.1:n.777+132A>C
NM_000212.2:c.777+132A>C , LRG_481t1:c.777+132A>C NP_000203.2:n.777+132A>C
NM_000212.3:c.777+132A>C MANE Select NP_000203.2:n.777+132A>C
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