Canonical Allele Identifier: CA8622984
Gene: ITGB3 HGNC NCBI

Linked Data

dbSNP Id: rs754655559
ExAC: 17:45362014 A / G
gnomAD v2: 17-45362014-A-G
gnomAD v3: 17-47284648-A-G
gnomAD v4: 17-47284648-A-G
MyVariant Identifiers: chr17:g.45362014A>G (hg19) chr17:g.47284648A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47284648A>G , CM000679.2:g.47284648A>G GRCh38
NC_000017.10:g.45362014A>G , CM000679.1:g.45362014A>G GRCh37
NC_000017.9:g.42717013A>G NCBI36
NG_008332.2:g.35807A>G , LRG_481:g.35807A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.567A>G ENSP00000513002.1:p.Pro189=
ENST00000559488.7:c.567A>G MANE Select ENSP00000452786.2:p.Pro189=
ENST00000559488.5:c.567A>G ENSP00000452786.1:p.Pro189=
ENST00000560629.1:c.532A>G
ENST00000571680.1:c.567A>G ENSP00000461626.1:p.Pro189=
NM_000212.2:c.567A>G , LRG_481t1:c.567A>G NP_000203.2:p.Pro189=
NM_000212.3:c.567A>G MANE Select NP_000203.2:p.Pro189=
Search 100 bp 5'
Search 100 bp 3'