Canonical Allele Identifier: CA2576291235
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44377667del , CM000679.2:g.44377667del GRCh38
NC_000017.10:g.42455035del , CM000679.1:g.42455035del GRCh37
NC_000017.9:g.39810561del NCBI36
NG_008331.1:g.16840del , LRG_479:g.16840del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.2187+32del MANE Select ENSP00000262407.5:n.2187+32del
ENST00000648408.1:c.1618+32del
ENST00000262407.5:c.2187+32del ENSP00000262407.5:n.2187+32del
ENST00000592462.5:n.982+32del
NM_000419.3:c.2187+32del , LRG_479t1:c.2187+32del NP_000410.2:n.2187+32del
XM_011524749.1:c.2187+32del XP_011523051.1:n.2187+32del
XM_011524750.1:c.2187+32del XP_011523052.1:n.2187+32del
NM_000419.4:c.2187+32del NP_000410.2:n.2187+32del
NM_000419.5:c.2187+32del MANE Select NP_000410.2:n.2187+32del