Canonical Allele Identifier: CA2261365311

Gene: ITGA2B

Linked Data

• dbSNP Id: rs2048522699

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374599_44374601del , CM000679.2:g.44374599_44374601del	GRCh38
NC_000017.10:g.42451967_42451969del , CM000679.1:g.42451967_42451969del	GRCh37
NC_000017.9:g.39807493_39807495del	NCBI36
NG_008331.1:g.19905_19907del , LRG_479:g.19905_19907del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2943+58_2943+60del MANE Select	ENSP00000262407.5:n.2943+58_2943+60del
ENST00000648408.1:c.2374+58_2374+60del
ENST00000262407.5:c.2943+58_2943+60del	ENSP00000262407.5:n.2943+58_2943+60del
ENST00000587295.5:c.253+1232_253+1234del
ENST00000588098.1:c.37+58_37+60del
ENST00000592462.5:n.2512_2514del
NM_000419.3:c.2943+58_2943+60del , LRG_479t1:c.2943+58_2943+60del	NP_000410.2:n.2943+58_2943+60del
XM_011524749.1:c.2842-131_2842-129del	XP_011523051.1:n.2842-131_2842-129del
XM_011524750.1:c.2943+58_2943+60del	XP_011523052.1:n.2943+58_2943+60del
NM_000419.4:c.2943+58_2943+60del	NP_000410.2:n.2943+58_2943+60del
NM_000419.5:c.2943+58_2943+60del MANE Select	NP_000410.2:n.2943+58_2943+60del