Canonical Allele Identifier: CA400023285

Gene: ITGB3

Linked Data

• dbSNP Id: rs1598690169
• MyVariant Identifiers: chr17:g.45362037A>C (hg19) ; chr17:g.47284671A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47284671A>C , CM000679.2:g.47284671A>C	GRCh38
NC_000017.10:g.45362037A>C , CM000679.1:g.45362037A>C	GRCh37
NC_000017.9:g.42717036A>C	NCBI36
NG_008332.2:g.35830A>C , LRG_481:g.35830A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696963.1:c.590A>C	ENSP00000513002.1:p.Glu197Ala
ENST00000559488.7:c.590A>C MANE Select	ENSP00000452786.2:p.Glu197Ala
ENST00000559488.5:c.590A>C	ENSP00000452786.1:p.Glu197Ala
ENST00000560629.1:c.555A>C
ENST00000571680.1:c.590A>C	ENSP00000461626.1:p.Glu197Ala
NM_000212.2:c.590A>C , LRG_481t1:c.590A>C	NP_000203.2:p.Glu197Ala
NM_000212.3:c.590A>C MANE Select	NP_000203.2:p.Glu197Ala