Canonical Allele Identifier: CA2261364484
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372666T= , CM000679.2:g.44372666T= GRCh38
NC_000017.10:g.42450034T= , CM000679.1:g.42450034T= GRCh37
NC_000017.9:g.39805560T= NCBI36
NG_008331.1:g.21840A= , LRG_479:g.21840A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3061-243A= MANE Select ENSP00000262407.5:n.3061-243A=
ENST00000648408.1:c.2375-243A=
ENST00000262407.5:c.3061-243A= ENSP00000262407.5:n.3061-243A=
ENST00000587295.5:c.254-243A=
ENST00000588098.1:c.38-243A=
NM_000419.3:c.3061-243A= , LRG_479t1:c.3061-243A= NP_000410.2:n.3061-243A=
XM_011524749.1:c.2959-243A= XP_011523051.1:n.2959-243A=
XM_011524750.1:c.2944-243A= XP_011523052.1:n.2944-243A=
NM_000419.4:c.3061-243A= NP_000410.2:n.3061-243A=
NM_000419.5:c.3061-243A= MANE Select NP_000410.2:n.3061-243A=