Canonical Allele Identifier: CA2638214819

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44374555-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374556del , CM000679.2:g.44374556del	GRCh38
NC_000017.10:g.42451924del , CM000679.1:g.42451924del	GRCh37
NC_000017.9:g.39807450del	NCBI36
NG_008331.1:g.19950del , LRG_479:g.19950del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2944-86del MANE Select	ENSP00000262407.5:n.2944-86del
ENST00000648408.1:c.2374+103del
ENST00000262407.5:c.2944-86del	ENSP00000262407.5:n.2944-86del
ENST00000587295.5:c.253+1277del
ENST00000588098.1:c.37+103del
ENST00000592462.5:n.2557del
NM_000419.3:c.2944-86del , LRG_479t1:c.2944-86del	NP_000410.2:n.2944-86del
XM_011524749.1:c.2842-86del	XP_011523051.1:n.2842-86del
XM_011524750.1:c.2943+103del	XP_011523052.1:n.2943+103del
NM_000419.4:c.2944-86del	NP_000410.2:n.2944-86del
NM_000419.5:c.2944-86del MANE Select	NP_000410.2:n.2944-86del