Canonical Allele Identifier: CA2261364334
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372339T= , CM000679.2:g.44372339T= GRCh38
NC_000017.10:g.42449707T= , CM000679.1:g.42449707T= GRCh37
NC_000017.9:g.39805233T= NCBI36
NG_008331.1:g.22167A= , LRG_479:g.22167A=

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.*25A= MANE Select ENSP00000262407.5:n.*25A=
ENST00000648408.1:c.2459A=
ENST00000262407.5:c.*25A= ENSP00000262407.5:n.*25A=
ENST00000587295.5:c.338A=
ENST00000588098.1:c.122A=
NM_000419.3:c.*25A= , LRG_479t1:c.*25A= NP_000410.2:n.*25A=
XM_011524749.1:c.*25A= XP_011523051.1:n.*25A=
XM_011524750.1:c.*25A= XP_011523052.1:n.*25A=
NM_000419.4:c.*25A= NP_000410.2:n.*25A=
NM_000419.5:c.*25A= MANE Select NP_000410.2:n.*25A=