Canonical Allele Identifier: CA2261364461
Gene: ITGA2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372602G= , CM000679.2:g.44372602G= GRCh38
NC_000017.10:g.42449970G= , CM000679.1:g.42449970G= GRCh37
NC_000017.9:g.39805496G= NCBI36
NG_008331.1:g.21904C= , LRG_479:g.21904C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3061-179C= MANE Select ENSP00000262407.5:n.3061-179C=
ENST00000648408.1:c.2375-179C=
ENST00000262407.5:c.3061-179C= ENSP00000262407.5:n.3061-179C=
ENST00000587295.5:c.254-179C=
ENST00000588098.1:c.38-179C=
NM_000419.3:c.3061-179C= , LRG_479t1:c.3061-179C= NP_000410.2:n.3061-179C=
XM_011524749.1:c.2959-179C= XP_011523051.1:n.2959-179C=
XM_011524750.1:c.2944-179C= XP_011523052.1:n.2944-179C=
NM_000419.4:c.3061-179C= NP_000410.2:n.3061-179C=
NM_000419.5:c.3061-179C= MANE Select NP_000410.2:n.3061-179C=
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