Canonical Allele Identifier: CA2261365507

Gene: ITGA2B

Linked Data

• dbSNP Id: rs2048526837

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374968_44374983del , CM000679.2:g.44374968_44374983del	GRCh38
NC_000017.10:g.42452336_42452351del , CM000679.1:g.42452336_42452351del	GRCh37
NC_000017.9:g.39807862_39807877del	NCBI36
NG_008331.1:g.19524_19539del , LRG_479:g.19524_19539del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2841+16_2841+31del MANE Select	ENSP00000262407.5:n.2841+16_2841+31del
ENST00000648408.1:c.2272+16_2272+31del
ENST00000262407.5:c.2841+16_2841+31del	ENSP00000262407.5:n.2841+16_2841+31del
ENST00000587295.5:c.253+851_253+866del
ENST00000592462.5:n.2131_2146del
NM_000419.3:c.2841+16_2841+31del , LRG_479t1:c.2841+16_2841+31del	NP_000410.2:n.2841+16_2841+31del
XM_011524749.1:c.2841+16_2841+31del	XP_011523051.1:n.2841+16_2841+31del
XM_011524750.1:c.2841+16_2841+31del	XP_011523052.1:n.2841+16_2841+31del
NM_000419.4:c.2841+16_2841+31del	NP_000410.2:n.2841+16_2841+31del
NM_000419.5:c.2841+16_2841+31del MANE Select	NP_000410.2:n.2841+16_2841+31del