Canonical Allele Identifier: CA291224913
Gene: ITGB3 HGNC NCBI

Linked Data

dbSNP Id: rs376931677
MyVariant Identifiers: chr17:g.45363915T>G (hg19) chr17:g.47286549T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47286549T>G , CM000679.2:g.47286549T>G GRCh38
NC_000017.10:g.45363915T>G , CM000679.1:g.45363915T>G GRCh37
NC_000017.9:g.42718914T>G NCBI36
NG_008332.2:g.37708T>G , LRG_481:g.37708T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.777+127T>G ENSP00000513002.1:n.777+127T>G
ENST00000559488.7:c.777+127T>G MANE Select ENSP00000452786.2:n.777+127T>G
ENST00000559488.5:c.777+127T>G ENSP00000452786.1:n.777+127T>G
ENST00000560629.1:c.742+127T>G
ENST00000571680.1:c.777+127T>G ENSP00000461626.1:n.777+127T>G
NM_000212.2:c.777+127T>G , LRG_481t1:c.777+127T>G NP_000203.2:n.777+127T>G
NM_000212.3:c.777+127T>G MANE Select NP_000203.2:n.777+127T>G
Search 100 bp 5'
Search 100 bp 3'