Canonical Allele Identifier: CA2638215061

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44374971-G-GCCCCCCCCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374975_44374976insCCCCCCCCCCC , CM000679.2:g.44374975_44374976insCCCCCCCCCCC	GRCh38
NC_000017.10:g.42452343_42452344insCCCCCCCCCCC , CM000679.1:g.42452343_42452344insCCCCCCCCCCC	GRCh37
NC_000017.9:g.39807869_39807870insCCCCCCCCCCC	NCBI36
NG_008331.1:g.19534_19535insGGGGGGGGGGG , LRG_479:g.19534_19535insGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2841+26_2841+27insGGGGGGGGGGG MANE Select	ENSP00000262407.5:n.2841+26_2841+27insGGGGGGGGGGG
ENST00000648408.1:c.2272+26_2272+27insGGGGGGGGGGG
ENST00000262407.5:c.2841+26_2841+27insGGGGGGGGGGG	ENSP00000262407.5:n.2841+26_2841+27insGGGGGGGGGGG
ENST00000587295.5:c.253+861_253+862insGGGGGGGGGGG
ENST00000592462.5:n.2141_2142insGGGGGGGGGGG
NM_000419.3:c.2841+26_2841+27insGGGGGGGGGGG , LRG_479t1:c.2841+26_2841+27insGGGGGGGGGGG	NP_000410.2:n.2841+26_2841+27insGGGGGGGGGGG
XM_011524749.1:c.2841+26_2841+27insGGGGGGGGGGG	XP_011523051.1:n.2841+26_2841+27insGGGGGGGGGGG
XM_011524750.1:c.2841+26_2841+27insGGGGGGGGGGG	XP_011523052.1:n.2841+26_2841+27insGGGGGGGGGGG
NM_000419.4:c.2841+26_2841+27insGGGGGGGGGGG	NP_000410.2:n.2841+26_2841+27insGGGGGGGGGGG
NM_000419.5:c.2841+26_2841+27insGGGGGGGGGGG MANE Select	NP_000410.2:n.2841+26_2841+27insGGGGGGGGGGG