Canonical Allele Identifier: CA2638213143
Gene: ITGA2B HGNC NCBI

Linked Data

gnomAD v4: 17-44372186-GC-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372187del , CM000679.2:g.44372187del GRCh38
NC_000017.10:g.42449555del , CM000679.1:g.42449555del GRCh37
NC_000017.9:g.39805081del NCBI36
NG_008331.1:g.22319del , LRG_479:g.22319del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.*177del MANE Select ENSP00000262407.5:n.*177del
ENST00000648408.1:c.2611del
ENST00000262407.5:c.*177del ENSP00000262407.5:n.*177del
ENST00000587295.5:c.490del
ENST00000588098.1:c.274del
NM_000419.3:c.*177del , LRG_479t1:c.*177del NP_000410.2:n.*177del
XM_011524749.1:c.*177del XP_011523051.1:n.*177del
XM_011524750.1:c.*177del XP_011523052.1:n.*177del
NM_000419.4:c.*177del NP_000410.2:n.*177del
NM_000419.5:c.*177del MANE Select NP_000410.2:n.*177del
Search 100 bp 5'
Search 100 bp 3'