Canonical Allele Identifier: CA626378187
Gene: ITGB3 HGNC NCBI

Linked Data

dbSNP Id: rs1187862792
gnomAD v2: 17-45361118-T-C
MyVariant Identifiers: chr17:g.45361118T>C (hg19) chr17:g.47283752T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47283752T>C , CM000679.2:g.47283752T>C GRCh38
NC_000017.10:g.45361118T>C , CM000679.1:g.45361118T>C GRCh37
NC_000017.9:g.42716117T>C NCBI36
NG_008332.2:g.34911T>C , LRG_481:g.34911T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.361+203T>C ENSP00000513002.1:n.361+203T>C
ENST00000559488.7:c.361+203T>C MANE Select ENSP00000452786.2:n.361+203T>C
ENST00000559488.5:c.361+203T>C ENSP00000452786.1:n.361+203T>C
ENST00000560629.1:c.326+203T>C
ENST00000571680.1:c.361+203T>C ENSP00000461626.1:n.361+203T>C
NM_000212.2:c.361+203T>C , LRG_481t1:c.361+203T>C NP_000203.2:n.361+203T>C
NM_000212.3:c.361+203T>C MANE Select NP_000203.2:n.361+203T>C
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