Canonical Allele Identifier: CA399787909
Gene: ITGA2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2572659
ClinVar RCV Id: RCV003314544

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372414A>T , CM000679.2:g.44372414A>T GRCh38
NC_000017.10:g.42449782A>T , CM000679.1:g.42449782A>T GRCh37
NC_000017.9:g.39805308A>T NCBI36
NG_008331.1:g.22092T>A , LRG_479:g.22092T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.3070T>A MANE Select ENSP00000262407.5:p.Phe1024Ile
ENST00000648408.1:c.2384T>A
ENST00000262407.5:c.3070T>A ENSP00000262407.5:p.Phe1024Ile
ENST00000587295.5:c.263T>A
ENST00000588098.1:c.47T>A
NM_000419.3:c.3070T>A , LRG_479t1:c.3070T>A NP_000410.2:p.Phe1024Ile
XM_011524749.1:c.2968T>A XP_011523051.1:p.Phe990Ile
XM_011524750.1:c.2953T>A XP_011523052.1:p.Phe985Ile
NM_000419.4:c.3070T>A NP_000410.2:p.Phe1024Ile
NM_000419.5:c.3070T>A MANE Select NP_000410.2:p.Phe1024Ile