Canonical Allele Identifier: CA2576290920
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44374918del , CM000679.2:g.44374918del GRCh38
NC_000017.10:g.42452286del , CM000679.1:g.42452286del GRCh37
NC_000017.9:g.39807812del NCBI36
NG_008331.1:g.19590del , LRG_479:g.19590del

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.2841+82del MANE Select ENSP00000262407.5:n.2841+82del
ENST00000648408.1:c.2272+82del
ENST00000262407.5:c.2841+82del ENSP00000262407.5:n.2841+82del
ENST00000587295.5:c.253+917del
ENST00000592462.5:n.2197del
NM_000419.3:c.2841+82del , LRG_479t1:c.2841+82del NP_000410.2:n.2841+82del
XM_011524749.1:c.2841+82del XP_011523051.1:n.2841+82del
XM_011524750.1:c.2841+82del XP_011523052.1:n.2841+82del
NM_000419.4:c.2841+82del NP_000410.2:n.2841+82del
NM_000419.5:c.2841+82del MANE Select NP_000410.2:n.2841+82del