Canonical Allele Identifier: CA772536150
Gene: ITGB3 HGNC NCBI

Linked Data

dbSNP Id: rs1316605353
gnomAD v4: 17-47284565-A-ACAC
MyVariant Identifiers: chr17:g.45361931_45361932insCAC (hg19) chr17:g.47284565_47284566insCAC (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47284566_47284567insACC , CM000679.2:g.47284566_47284567insACC GRCh38
NC_000017.10:g.45361932_45361933insACC , CM000679.1:g.45361932_45361933insACC GRCh37
NC_000017.9:g.42716931_42716932insACC NCBI36
NG_008332.2:g.35725_35726insACC , LRG_481:g.35725_35726insACC

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.485_486insACC ENSP00000513002.1:p.Thr162_Lys163insPro
ENST00000559488.7:c.485_486insACC MANE Select ENSP00000452786.2:p.Thr162_Lys163insPro
ENST00000559488.5:c.485_486insACC ENSP00000452786.1:p.Thr162_Lys163insPro
ENST00000560629.1:c.450_451insACC
ENST00000571680.1:c.485_486insACC ENSP00000461626.1:p.Thr162_Lys163insPro
NM_000212.2:c.485_486insACC , LRG_481t1:c.485_486insACC NP_000203.2:p.Thr162_Lys163insPro
NM_000212.3:c.485_486insACC MANE Select NP_000203.2:p.Thr162_Lys163insPro
Search 100 bp 5'
Search 100 bp 3'