Canonical Allele Identifier: CA500432028
Gene: ITGB3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.45363749G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47286383G>A , CM000679.2:g.47286383G>A GRCh38
NC_000017.10:g.45363749G>A , CM000679.1:g.45363749G>A GRCh37
NC_000017.9:g.42718748G>A NCBI36
NG_008332.2:g.37542G>A , LRG_481:g.37542G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.738G>A ENSP00000513002.1:p.Glu246=
ENST00000559488.7:c.738G>A MANE Select ENSP00000452786.2:p.Glu246=
ENST00000559488.5:c.738G>A ENSP00000452786.1:p.Glu246=
ENST00000560629.1:c.703G>A
ENST00000571680.1:c.738G>A ENSP00000461626.1:p.Glu246=
NM_000212.2:c.738G>A , LRG_481t1:c.738G>A NP_000203.2:p.Glu246=
NM_000212.3:c.738G>A MANE Select NP_000203.2:p.Glu246=