Canonical Allele Identifier: CA399787674
Gene: ITGA2B HGNC NCBI

Linked Data

dbSNP Id: rs2048504649

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372379A>T , CM000679.2:g.44372379A>T GRCh38
NC_000017.10:g.42449747A>T , CM000679.1:g.42449747A>T GRCh37
NC_000017.9:g.39805273A>T NCBI36
NG_008331.1:g.22127T>A , LRG_479:g.22127T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3105T>A MANE Select ENSP00000262407.5:p.Asp1035Glu
ENST00000648408.1:c.2419T>A
ENST00000262407.5:c.3105T>A ENSP00000262407.5:p.Asp1035Glu
ENST00000587295.5:c.298T>A
ENST00000588098.1:c.82T>A
NM_000419.3:c.3105T>A , LRG_479t1:c.3105T>A NP_000410.2:p.Asp1035Glu
XM_011524749.1:c.3003T>A XP_011523051.1:p.Asp1001Glu
XM_011524750.1:c.2988T>A XP_011523052.1:p.Asp996Glu
NM_000419.4:c.3105T>A NP_000410.2:p.Asp1035Glu
NM_000419.5:c.3105T>A MANE Select NP_000410.2:p.Asp1035Glu