Canonical Allele Identifier: CA400020750

Gene: ITGB3

Linked Data

• MyVariant Identifiers: chr17:g.45360831A>T (hg19) ; chr17:g.47283465A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47283465A>T , CM000679.2:g.47283465A>T	GRCh38
NC_000017.10:g.45360831A>T , CM000679.1:g.45360831A>T	GRCh37
NC_000017.9:g.42715830A>T	NCBI36
NG_008332.2:g.34624A>T , LRG_481:g.34624A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696963.1:c.277A>T	ENSP00000513002.1:p.Arg93Trp
ENST00000559488.7:c.277A>T MANE Select	ENSP00000452786.2:p.Arg93Trp
ENST00000559488.5:c.277A>T	ENSP00000452786.1:p.Arg93Trp
ENST00000560629.1:c.242A>T
ENST00000571680.1:c.277A>T	ENSP00000461626.1:p.Arg93Trp
NM_000212.2:c.277A>T , LRG_481t1:c.277A>T	NP_000203.2:p.Arg93Trp
NM_000212.3:c.277A>T MANE Select	NP_000203.2:p.Arg93Trp