Canonical Allele Identifier: CA2576290879

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44374558-GCCAC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374565_44374568del , CM000679.2:g.44374565_44374568del	GRCh38
NC_000017.10:g.42451933_42451936del , CM000679.1:g.42451933_42451936del	GRCh37
NC_000017.9:g.39807459_39807462del	NCBI36
NG_008331.1:g.19944_19947del , LRG_479:g.19944_19947del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2944-92_2944-89del MANE Select	ENSP00000262407.5:n.2944-92_2944-89del
ENST00000648408.1:c.2374+97_2374+100del
ENST00000262407.5:c.2944-92_2944-89del	ENSP00000262407.5:n.2944-92_2944-89del
ENST00000587295.5:c.253+1271_253+1274del
ENST00000588098.1:c.37+97_37+100del
ENST00000592462.5:n.2551_2554del
NM_000419.3:c.2944-92_2944-89del , LRG_479t1:c.2944-92_2944-89del	NP_000410.2:n.2944-92_2944-89del
XM_011524749.1:c.2842-92_2842-89del	XP_011523051.1:n.2842-92_2842-89del
XM_011524750.1:c.2943+97_2943+100del	XP_011523052.1:n.2943+97_2943+100del
NM_000419.4:c.2944-92_2944-89del	NP_000410.2:n.2944-92_2944-89del
NM_000419.5:c.2944-92_2944-89del MANE Select	NP_000410.2:n.2944-92_2944-89del