Canonical Allele Identifier: CA400020762
Gene: ITGB3 HGNC NCBI

Linked Data

dbSNP Id: rs1180530619

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47283467G>T , CM000679.2:g.47283467G>T GRCh38
NC_000017.10:g.45360833G>T , CM000679.1:g.45360833G>T GRCh37
NC_000017.9:g.42715832G>T NCBI36
NG_008332.2:g.34626G>T , LRG_481:g.34626G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.279G>T ENSP00000513002.1:p.Arg93Ser
ENST00000559488.7:c.279G>T MANE Select ENSP00000452786.2:p.Arg93Ser
ENST00000559488.5:c.279G>T ENSP00000452786.1:p.Arg93Ser
ENST00000560629.1:c.244G>T
ENST00000571680.1:c.279G>T ENSP00000461626.1:p.Arg93Ser
NM_000212.2:c.279G>T , LRG_481t1:c.279G>T NP_000203.2:p.Arg93Ser
NM_000212.3:c.279G>T MANE Select NP_000203.2:p.Arg93Ser