Canonical Allele Identifier: CA2638214808

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44374537-A-AGGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374540_44374543dup , CM000679.2:g.44374540_44374543dup	GRCh38
NC_000017.10:g.42451908_42451911dup , CM000679.1:g.42451908_42451911dup	GRCh37
NC_000017.9:g.39807434_39807437dup	NCBI36
NG_008331.1:g.19965_19968dup , LRG_479:g.19965_19968dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2944-71_2944-68dup MANE Select	ENSP00000262407.5:n.2944-71_2944-68dup
ENST00000648408.1:c.2374+118_2374+121dup
ENST00000262407.5:c.2944-71_2944-68dup	ENSP00000262407.5:n.2944-71_2944-68dup
ENST00000587295.5:c.253+1292_253+1295dup
ENST00000588098.1:c.37+118_37+121dup
ENST00000592462.5:n.2572_2575dup
NM_000419.3:c.2944-71_2944-68dup , LRG_479t1:c.2944-71_2944-68dup	NP_000410.2:n.2944-71_2944-68dup
XM_011524749.1:c.2842-71_2842-68dup	XP_011523051.1:n.2842-71_2842-68dup
XM_011524750.1:c.2943+118_2943+121dup	XP_011523052.1:n.2943+118_2943+121dup
NM_000419.4:c.2944-71_2944-68dup	NP_000410.2:n.2944-71_2944-68dup
NM_000419.5:c.2944-71_2944-68dup MANE Select	NP_000410.2:n.2944-71_2944-68dup