Canonical Allele Identifier: CA2638213299

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44372240-GGAAAC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44372243_44372247del , CM000679.2:g.44372243_44372247del	GRCh38
NC_000017.10:g.42449611_42449615del , CM000679.1:g.42449611_42449615del	GRCh37
NC_000017.9:g.39805137_39805141del	NCBI36
NG_008331.1:g.22261_22265del , LRG_479:g.22261_22265del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.*119_*123del MANE Select	ENSP00000262407.5:n.*119_*123del
ENST00000648408.1:c.2553_2557del
ENST00000262407.5:c.*119_*123del	ENSP00000262407.5:n.*119_*123del
ENST00000587295.5:c.432_436del
ENST00000588098.1:c.216_220del
NM_000419.3:c.*119_*123del , LRG_479t1:c.*119_*123del	NP_000410.2:n.*119_*123del
XM_011524749.1:c.*119_*123del	XP_011523051.1:n.*119_*123del
XM_011524750.1:c.*119_*123del	XP_011523052.1:n.*119_*123del
NM_000419.4:c.*119_*123del	NP_000410.2:n.*119_*123del
NM_000419.5:c.*119_*123del MANE Select	NP_000410.2:n.*119_*123del