Canonical Allele Identifier: CA2638214866

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44374785-G-GGC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374785_44374786insGC , CM000679.2:g.44374785_44374786insGC	GRCh38
NC_000017.10:g.42452153_42452154insGC , CM000679.1:g.42452153_42452154insGC	GRCh37
NC_000017.9:g.39807679_39807680insGC	NCBI36
NG_008331.1:g.19720_19721insGC , LRG_479:g.19720_19721insGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2842-26_2842-25insGC MANE Select	ENSP00000262407.5:n.2842-26_2842-25insGC
ENST00000648408.1:c.2273-26_2273-25insGC
ENST00000262407.5:c.2842-26_2842-25insGC	ENSP00000262407.5:n.2842-26_2842-25insGC
ENST00000587295.5:c.253+1047_253+1048insGC
ENST00000592462.5:n.2327_2328insGC
NM_000419.3:c.2842-26_2842-25insGC , LRG_479t1:c.2842-26_2842-25insGC	NP_000410.2:n.2842-26_2842-25insGC
XM_011524749.1:c.2841+212_2841+213insGC	XP_011523051.1:n.2841+212_2841+213insGC
XM_011524750.1:c.2842-26_2842-25insGC	XP_011523052.1:n.2842-26_2842-25insGC
NM_000419.4:c.2842-26_2842-25insGC	NP_000410.2:n.2842-26_2842-25insGC
NM_000419.5:c.2842-26_2842-25insGC MANE Select	NP_000410.2:n.2842-26_2842-25insGC