Canonical Allele Identifier: CA2261364410
Gene: ITGA2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372484T= , CM000679.2:g.44372484T= GRCh38
NC_000017.10:g.42449852T= , CM000679.1:g.42449852T= GRCh37
NC_000017.9:g.39805378T= NCBI36
NG_008331.1:g.22022A= , LRG_479:g.22022A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3061-61A= MANE Select ENSP00000262407.5:n.3061-61A=
ENST00000648408.1:c.2375-61A=
ENST00000262407.5:c.3061-61A= ENSP00000262407.5:n.3061-61A=
ENST00000587295.5:c.254-61A=
ENST00000588098.1:c.38-61A=
NM_000419.3:c.3061-61A= , LRG_479t1:c.3061-61A= NP_000410.2:n.3061-61A=
XM_011524749.1:c.2959-61A= XP_011523051.1:n.2959-61A=
XM_011524750.1:c.2944-61A= XP_011523052.1:n.2944-61A=
NM_000419.4:c.3061-61A= NP_000410.2:n.3061-61A=
NM_000419.5:c.3061-61A= MANE Select NP_000410.2:n.3061-61A=
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