Canonical Allele Identifier: CA626684813
Gene: ITGB3 HGNC NCBI

Linked Data

dbSNP Id: rs1290620962
gnomAD v2: 17-45360461-C-T
gnomAD v3: 17-47283095-C-T
gnomAD v4: 17-47283095-C-T
MyVariant Identifiers: chr17:g.45360461C>T (hg19) chr17:g.47283095C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47283095C>T , CM000679.2:g.47283095C>T GRCh38
NC_000017.10:g.45360461C>T , CM000679.1:g.45360461C>T GRCh37
NC_000017.9:g.42715460C>T NCBI36
NG_008332.2:g.34254C>T , LRG_481:g.34254C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.166-259C>T ENSP00000513002.1:n.166-259C>T
ENST00000559488.7:c.166-259C>T MANE Select ENSP00000452786.2:n.166-259C>T
ENST00000559488.5:c.166-259C>T ENSP00000452786.1:n.166-259C>T
ENST00000560629.1:c.131-259C>T
ENST00000571680.1:c.166-259C>T ENSP00000461626.1:n.166-259C>T
NM_000212.2:c.166-259C>T , LRG_481t1:c.166-259C>T NP_000203.2:n.166-259C>T
NM_000212.3:c.166-259C>T MANE Select NP_000203.2:n.166-259C>T
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