Canonical Allele Identifier: CA2576290912
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44374829del , CM000679.2:g.44374829del GRCh38
NC_000017.10:g.42452197del , CM000679.1:g.42452197del GRCh37
NC_000017.9:g.39807723del NCBI36
NG_008331.1:g.19679del , LRG_479:g.19679del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.2842-67del MANE Select ENSP00000262407.5:n.2842-67del
ENST00000648408.1:c.2273-67del
ENST00000262407.5:c.2842-67del ENSP00000262407.5:n.2842-67del
ENST00000587295.5:c.253+1006del
ENST00000592462.5:n.2286del
NM_000419.3:c.2842-67del , LRG_479t1:c.2842-67del NP_000410.2:n.2842-67del
XM_011524749.1:c.2841+171del XP_011523051.1:n.2841+171del
XM_011524750.1:c.2842-67del XP_011523052.1:n.2842-67del
NM_000419.4:c.2842-67del NP_000410.2:n.2842-67del
NM_000419.5:c.2842-67del MANE Select NP_000410.2:n.2842-67del