Canonical Allele Identifier: CA400021531

Gene: ITGB3

Linked Data

• MyVariant Identifiers: chr17:g.45361808G>T (hg19) ; chr17:g.47284442G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47284442G>T , CM000679.2:g.47284442G>T	GRCh38
NC_000017.10:g.45361808G>T , CM000679.1:g.45361808G>T	GRCh37
NC_000017.9:g.42716807G>T	NCBI36
NG_008332.2:g.35601G>T , LRG_481:g.35601G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696963.1:c.362-1G>T	ENSP00000513002.1:n.362-1G>T
ENST00000559488.7:c.362-1G>T MANE Select	ENSP00000452786.2:n.362-1G>T
ENST00000559488.5:c.362-1G>T	ENSP00000452786.1:n.362-1G>T
ENST00000560629.1:c.327-1G>T
ENST00000571680.1:c.362-1G>T	ENSP00000461626.1:n.362-1G>T
NM_000212.2:c.362-1G>T , LRG_481t1:c.362-1G>T	NP_000203.2:n.362-1G>T
NM_000212.3:c.362-1G>T MANE Select	NP_000203.2:n.362-1G>T