Canonical Allele Identifier: CA2261364263
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372213G= , CM000679.2:g.44372213G= GRCh38
NC_000017.10:g.42449581G= , CM000679.1:g.42449581G= GRCh37
NC_000017.9:g.39805107G= NCBI36
NG_008331.1:g.22293C= , LRG_479:g.22293C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.*151C= MANE Select ENSP00000262407.5:n.*151C=
ENST00000648408.1:c.2585C=
ENST00000262407.5:c.*151C= ENSP00000262407.5:n.*151C=
ENST00000587295.5:c.464C=
ENST00000588098.1:c.248C=
NM_000419.3:c.*151C= , LRG_479t1:c.*151C= NP_000410.2:n.*151C=
XM_011524749.1:c.*151C= XP_011523051.1:n.*151C=
XM_011524750.1:c.*151C= XP_011523052.1:n.*151C=
NM_000419.4:c.*151C= NP_000410.2:n.*151C=
NM_000419.5:c.*151C= MANE Select NP_000410.2:n.*151C=