Canonical Allele Identifier: CA2638215010

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44374952-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374952_44374953insG , CM000679.2:g.44374952_44374953insG	GRCh38
NC_000017.10:g.42452320_42452321insG , CM000679.1:g.42452320_42452321insG	GRCh37
NC_000017.9:g.39807846_39807847insG	NCBI36
NG_008331.1:g.19553_19554insC , LRG_479:g.19553_19554insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.2841+45_2841+46insC MANE Select	ENSP00000262407.5:n.2841+45_2841+46insC
ENST00000648408.1:c.2272+45_2272+46insC
ENST00000262407.5:c.2841+45_2841+46insC	ENSP00000262407.5:n.2841+45_2841+46insC
ENST00000587295.5:c.253+880_253+881insC
ENST00000592462.5:n.2160_2161insC
NM_000419.3:c.2841+45_2841+46insC , LRG_479t1:c.2841+45_2841+46insC	NP_000410.2:n.2841+45_2841+46insC
XM_011524749.1:c.2841+45_2841+46insC	XP_011523051.1:n.2841+45_2841+46insC
XM_011524750.1:c.2841+45_2841+46insC	XP_011523052.1:n.2841+45_2841+46insC
NM_000419.4:c.2841+45_2841+46insC	NP_000410.2:n.2841+45_2841+46insC
NM_000419.5:c.2841+45_2841+46insC MANE Select	NP_000410.2:n.2841+45_2841+46insC