Canonical Allele Identifier: CA2638215095

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44374985-CGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374986_44374987del , CM000679.2:g.44374986_44374987del	GRCh38
NC_000017.10:g.42452354_42452355del , CM000679.1:g.42452354_42452355del	GRCh37
NC_000017.9:g.39807880_39807881del	NCBI36
NG_008331.1:g.19519_19520del , LRG_479:g.19519_19520del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2841+11_2841+12del MANE Select	ENSP00000262407.5:n.2841+11_2841+12del
ENST00000648408.1:c.2272+11_2272+12del
ENST00000262407.5:c.2841+11_2841+12del	ENSP00000262407.5:n.2841+11_2841+12del
ENST00000587295.5:c.253+846_253+847del
ENST00000592462.5:n.2126_2127del
NM_000419.3:c.2841+11_2841+12del , LRG_479t1:c.2841+11_2841+12del	NP_000410.2:n.2841+11_2841+12del
XM_011524749.1:c.2841+11_2841+12del	XP_011523051.1:n.2841+11_2841+12del
XM_011524750.1:c.2841+11_2841+12del	XP_011523052.1:n.2841+11_2841+12del
NM_000419.4:c.2841+11_2841+12del	NP_000410.2:n.2841+11_2841+12del
NM_000419.5:c.2841+11_2841+12del MANE Select	NP_000410.2:n.2841+11_2841+12del