Canonical Allele Identifier: CA2638215030

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44374962-GAAGGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374963_44374967del , CM000679.2:g.44374963_44374967del	GRCh38
NC_000017.10:g.42452331_42452335del , CM000679.1:g.42452331_42452335del	GRCh37
NC_000017.9:g.39807857_39807861del	NCBI36
NG_008331.1:g.19539_19543del , LRG_479:g.19539_19543del

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.2841+31_2841+35del MANE Select	ENSP00000262407.5:n.2841+31_2841+35del
ENST00000648408.1:c.2272+31_2272+35del
ENST00000262407.5:c.2841+31_2841+35del	ENSP00000262407.5:n.2841+31_2841+35del
ENST00000587295.5:c.253+866_253+870del
ENST00000592462.5:n.2146_2150del
NM_000419.3:c.2841+31_2841+35del , LRG_479t1:c.2841+31_2841+35del	NP_000410.2:n.2841+31_2841+35del
XM_011524749.1:c.2841+31_2841+35del	XP_011523051.1:n.2841+31_2841+35del
XM_011524750.1:c.2841+31_2841+35del	XP_011523052.1:n.2841+31_2841+35del
NM_000419.4:c.2841+31_2841+35del	NP_000410.2:n.2841+31_2841+35del
NM_000419.5:c.2841+31_2841+35del MANE Select	NP_000410.2:n.2841+31_2841+35del