Canonical Allele Identifier: CA2576290835
Gene: ITGA2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372475del , CM000679.2:g.44372475del GRCh38
NC_000017.10:g.42449843del , CM000679.1:g.42449843del GRCh37
NC_000017.9:g.39805369del NCBI36
NG_008331.1:g.22034del , LRG_479:g.22034del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3061-49del MANE Select ENSP00000262407.5:n.3061-49del
ENST00000648408.1:c.2375-49del
ENST00000262407.5:c.3061-49del ENSP00000262407.5:n.3061-49del
ENST00000587295.5:c.254-49del
ENST00000588098.1:c.38-49del
NM_000419.3:c.3061-49del , LRG_479t1:c.3061-49del NP_000410.2:n.3061-49del
XM_011524749.1:c.2959-49del XP_011523051.1:n.2959-49del
XM_011524750.1:c.2944-49del XP_011523052.1:n.2944-49del
NM_000419.4:c.3061-49del NP_000410.2:n.3061-49del
NM_000419.5:c.3061-49del MANE Select NP_000410.2:n.3061-49del
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