Canonical Allele Identifier: CA2638214883

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44374823-AGGTCCCACACCCCC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374826_44374839del , CM000679.2:g.44374826_44374839del	GRCh38
NC_000017.10:g.42452194_42452207del , CM000679.1:g.42452194_42452207del	GRCh37
NC_000017.9:g.39807720_39807733del	NCBI36
NG_008331.1:g.19669_19682del , LRG_479:g.19669_19682del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2842-77_2842-64del MANE Select	ENSP00000262407.5:n.2842-77_2842-64del
ENST00000648408.1:c.2273-77_2273-64del
ENST00000262407.5:c.2842-77_2842-64del	ENSP00000262407.5:n.2842-77_2842-64del
ENST00000587295.5:c.253+996_253+1009del
ENST00000592462.5:n.2276_2289del
NM_000419.3:c.2842-77_2842-64del , LRG_479t1:c.2842-77_2842-64del	NP_000410.2:n.2842-77_2842-64del
XM_011524749.1:c.2841+161_2841+174del	XP_011523051.1:n.2841+161_2841+174del
XM_011524750.1:c.2842-77_2842-64del	XP_011523052.1:n.2842-77_2842-64del
NM_000419.4:c.2842-77_2842-64del	NP_000410.2:n.2842-77_2842-64del
NM_000419.5:c.2842-77_2842-64del MANE Select	NP_000410.2:n.2842-77_2842-64del