Canonical Allele Identifier: CA400023210

Gene: ITGB3

Linked Data

• MyVariant Identifiers: chr17:g.45362012C>G (hg19) ; chr17:g.47284646C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47284646C>G , CM000679.2:g.47284646C>G	GRCh38
NC_000017.10:g.45362012C>G , CM000679.1:g.45362012C>G	GRCh37
NC_000017.9:g.42717011C>G	NCBI36
NG_008332.2:g.35805C>G , LRG_481:g.35805C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696963.1:c.565C>G	ENSP00000513002.1:p.Pro189Ala
ENST00000559488.7:c.565C>G MANE Select	ENSP00000452786.2:p.Pro189Ala
ENST00000559488.5:c.565C>G	ENSP00000452786.1:p.Pro189Ala
ENST00000560629.1:c.530C>G
ENST00000571680.1:c.565C>G	ENSP00000461626.1:p.Pro189Ala
NM_000212.2:c.565C>G , LRG_481t1:c.565C>G	NP_000203.2:p.Pro189Ala
NM_000212.3:c.565C>G MANE Select	NP_000203.2:p.Pro189Ala