Canonical Allele Identifier: CA2638215018

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44374958-CCCAGAAGGCCCGGCCCCG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374961_44374978del , CM000679.2:g.44374961_44374978del	GRCh38
NC_000017.10:g.42452329_42452346del , CM000679.1:g.42452329_42452346del	GRCh37
NC_000017.9:g.39807855_39807872del	NCBI36
NG_008331.1:g.19530_19547del , LRG_479:g.19530_19547del

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.2841+22_2841+39del MANE Select	ENSP00000262407.5:n.2841+22_2841+39del
ENST00000648408.1:c.2272+22_2272+39del
ENST00000262407.5:c.2841+22_2841+39del	ENSP00000262407.5:n.2841+22_2841+39del
ENST00000587295.5:c.253+857_253+874del
ENST00000592462.5:n.2137_2154del
NM_000419.3:c.2841+22_2841+39del , LRG_479t1:c.2841+22_2841+39del	NP_000410.2:n.2841+22_2841+39del
XM_011524749.1:c.2841+22_2841+39del	XP_011523051.1:n.2841+22_2841+39del
XM_011524750.1:c.2841+22_2841+39del	XP_011523052.1:n.2841+22_2841+39del
NM_000419.4:c.2841+22_2841+39del	NP_000410.2:n.2841+22_2841+39del
NM_000419.5:c.2841+22_2841+39del MANE Select	NP_000410.2:n.2841+22_2841+39del