Canonical Allele Identifier: CA2261364256
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372206A= , CM000679.2:g.44372206A= GRCh38
NC_000017.10:g.42449574A= , CM000679.1:g.42449574A= GRCh37
NC_000017.9:g.39805100A= NCBI36
NG_008331.1:g.22300T= , LRG_479:g.22300T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.*158T= MANE Select ENSP00000262407.5:n.*158T=
ENST00000648408.1:c.2592T=
ENST00000262407.5:c.*158T= ENSP00000262407.5:n.*158T=
ENST00000587295.5:c.471T=
ENST00000588098.1:c.255T=
NM_000419.3:c.*158T= , LRG_479t1:c.*158T= NP_000410.2:n.*158T=
XM_011524749.1:c.*158T= XP_011523051.1:n.*158T=
XM_011524750.1:c.*158T= XP_011523052.1:n.*158T=
NM_000419.4:c.*158T= NP_000410.2:n.*158T=
NM_000419.5:c.*158T= MANE Select NP_000410.2:n.*158T=