Canonical Allele Identifier: CA2638214832

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44374584-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374588del , CM000679.2:g.44374588del	GRCh38
NC_000017.10:g.42451956del , CM000679.1:g.42451956del	GRCh37
NC_000017.9:g.39807482del	NCBI36
NG_008331.1:g.19921del , LRG_479:g.19921del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2943+74del MANE Select	ENSP00000262407.5:n.2943+74del
ENST00000648408.1:c.2374+74del
ENST00000262407.5:c.2943+74del	ENSP00000262407.5:n.2943+74del
ENST00000587295.5:c.253+1248del
ENST00000588098.1:c.37+74del
ENST00000592462.5:n.2528del
NM_000419.3:c.2943+74del , LRG_479t1:c.2943+74del	NP_000410.2:n.2943+74del
XM_011524749.1:c.2842-115del	XP_011523051.1:n.2842-115del
XM_011524750.1:c.2943+74del	XP_011523052.1:n.2943+74del
NM_000419.4:c.2943+74del	NP_000410.2:n.2943+74del
NM_000419.5:c.2943+74del MANE Select	NP_000410.2:n.2943+74del