Canonical Allele Identifier: CA2638213207

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44372212-A-AGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44372217_44372219dup , CM000679.2:g.44372217_44372219dup	GRCh38
NC_000017.10:g.42449585_42449587dup , CM000679.1:g.42449585_42449587dup	GRCh37
NC_000017.9:g.39805111_39805113dup	NCBI36
NG_008331.1:g.22291_22293dup , LRG_479:g.22291_22293dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.*149_*151dup MANE Select	ENSP00000262407.5:n.*149_*151dup
ENST00000648408.1:c.2583_2585dup
ENST00000262407.5:c.*149_*151dup	ENSP00000262407.5:n.*149_*151dup
ENST00000587295.5:c.462_464dup
ENST00000588098.1:c.246_248dup
NM_000419.3:c.*149_*151dup , LRG_479t1:c.*149_*151dup	NP_000410.2:n.*149_*151dup
XM_011524749.1:c.*149_*151dup	XP_011523051.1:n.*149_*151dup
XM_011524750.1:c.*149_*151dup	XP_011523052.1:n.*149_*151dup
NM_000419.4:c.*149_*151dup	NP_000410.2:n.*149_*151dup
NM_000419.5:c.*149_*151dup MANE Select	NP_000410.2:n.*149_*151dup