Canonical Allele Identifier: CA2261364323
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372321T= , CM000679.2:g.44372321T= GRCh38
NC_000017.10:g.42449689T= , CM000679.1:g.42449689T= GRCh37
NC_000017.9:g.39805215T= NCBI36
NG_008331.1:g.22185A= , LRG_479:g.22185A=

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.*43A= MANE Select ENSP00000262407.5:n.*43A=
ENST00000648408.1:c.2477A=
ENST00000262407.5:c.*43A= ENSP00000262407.5:n.*43A=
ENST00000587295.5:c.356A=
ENST00000588098.1:c.140A=
NM_000419.3:c.*43A= , LRG_479t1:c.*43A= NP_000410.2:n.*43A=
XM_011524749.1:c.*43A= XP_011523051.1:n.*43A=
XM_011524750.1:c.*43A= XP_011523052.1:n.*43A=
NM_000419.4:c.*43A= NP_000410.2:n.*43A=
NM_000419.5:c.*43A= MANE Select NP_000410.2:n.*43A=