Canonical Allele Identifier: CA2576290932
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44374956del , CM000679.2:g.44374956del GRCh38
NC_000017.10:g.42452324del , CM000679.1:g.42452324del GRCh37
NC_000017.9:g.39807850del NCBI36
NG_008331.1:g.19553del , LRG_479:g.19553del

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.2841+45del MANE Select ENSP00000262407.5:n.2841+45del
ENST00000648408.1:c.2272+45del
ENST00000262407.5:c.2841+45del ENSP00000262407.5:n.2841+45del
ENST00000587295.5:c.253+880del
ENST00000592462.5:n.2160del
NM_000419.3:c.2841+45del , LRG_479t1:c.2841+45del NP_000410.2:n.2841+45del
XM_011524749.1:c.2841+45del XP_011523051.1:n.2841+45del
XM_011524750.1:c.2841+45del XP_011523052.1:n.2841+45del
NM_000419.4:c.2841+45del NP_000410.2:n.2841+45del
NM_000419.5:c.2841+45del MANE Select NP_000410.2:n.2841+45del