Canonical Allele Identifier: CA2261365905

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44375704_44375705delinsGC , CM000679.2:g.44375704_44375705delinsGC	GRCh38
NC_000017.10:g.42453072_42453073delinsGC , CM000679.1:g.42453072_42453073delinsGC	GRCh37
NC_000017.9:g.39808598_39808599delinsGC	NCBI36
NG_008331.1:g.18801_18802delinsGC , LRG_479:g.18801_18802delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.2613_2614delinsGC MANE Select	ENSP00000262407.5:p.Gly871=
ENST00000648408.1:c.2044_2045delinsGC
ENST00000262407.5:c.2613_2614delinsGC	ENSP00000262407.5:p.Gly871=
ENST00000587295.5:c.253+128_253+129delinsGC
ENST00000592462.5:n.1408_1409delinsGC
NM_000419.3:c.2613_2614delinsGC , LRG_479t1:c.2613_2614delinsGC	NP_000410.2:p.Gly871=
XM_011524749.1:c.2613_2614delinsGC	XP_011523051.1:p.Gly871=
XM_011524750.1:c.2613_2614delinsGC	XP_011523052.1:p.Gly871=
NM_000419.4:c.2613_2614delinsGC	NP_000410.2:p.Gly871=
NM_000419.5:c.2613_2614delinsGC MANE Select	NP_000410.2:p.Gly871=