Canonical Allele Identifier: CA2391873696

Gene: ITGB2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44889180_44889218delinsAGGTGCTCACTGGGGTCCCCGAGTGAGCCCGGCTGCTGG , CM000683.2:g.44889180_44889218delinsAGGTGCTCACTGGGGTCCCCGAGTGAGCCCGGCTGCTGG	GRCh38
NC_000021.8:g.46309095_46309133delinsAGGTGCTCACTGGGGTCCCCGAGTGAGCCCGGCTGCTGG , CM000683.1:g.46309095_46309133delinsAGGTGCTCACTGGGGTCCCCGAGTGAGCCCGGCTGCTGG	GRCh37
NC_000021.7:g.45133523_45133561delinsAGGTGCTCACTGGGGTCCCCGAGTGAGCCCGGCTGCTGG	NCBI36
NG_007270.2:g.44621_44659delinsCCAGCAGCCGGGCTCACTCGGGGACCCCAGTGAGCACCT , LRG_76:g.44621_44659delinsCCAGCAGCCGGGCTCACTCGGGGACCCCAGTGAGCACCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696946.1:n.1084+58_1084+96delinsCCAGCAGCCGGGCTCACTCGGGGACCCCAGTGAGCACCT
ENST00000302347.10:c.1949+58_1949+96delinsCCAGCAGCCGGGCTCACTCGGGGACCCCAGTGAGCACCT	ENSP00000303242.6:n.1949+58_1949+96delinsCCAGCAGCCGGGCTCACTCG...
ENST00000652462.1:c.1877+58_1877+96delinsCCAGCAGCCGGGCTCACTCGGGGACCCCAGTGAGCACCT MANE Select	ENSP00000498780.1:n.1877+58_1877+96delinsCCAGCAGCCGGGCTCACTCG...
ENST00000302347.9:c.1877+58_1877+96delinsCCAGCAGCCGGGCTCACTCGGGGACCCCAGTGAGCACCT	ENSP00000303242.5:n.1877+58_1877+96delinsCCAGCAGCCGGGCTCACTCG...
ENST00000355153.8:c.1877+58_1877+96delinsCCAGCAGCCGGGCTCACTCGGGGACCCCAGTGAGCACCT	ENSP00000347279.4:n.1877+58_1877+96delinsCCAGCAGCCGGGCTCACTCG...
ENST00000397850.6:c.1877+58_1877+96delinsCCAGCAGCCGGGCTCACTCGGGGACCCCAGTGAGCACCT	ENSP00000380948.2:n.1877+58_1877+96delinsCCAGCAGCCGGGCTCACTCG...
ENST00000397852.5:c.1877+58_1877+96delinsCCAGCAGCCGGGCTCACTCGGGGACCCCAGTGAGCACCT	ENSP00000380950.1:n.1877+58_1877+96delinsCCAGCAGCCGGGCTCACTCG...
ENST00000397854.7:c.1706+58_1706+96delinsCCAGCAGCCGGGCTCACTCGGGGACCCCAGTGAGCACCT	ENSP00000380952.3:n.1706+58_1706+96delinsCCAGCAGCCGGGCTCACTCG...
ENST00000397857.5:c.1877+58_1877+96delinsCCAGCAGCCGGGCTCACTCGGGGACCCCAGTGAGCACCT	ENSP00000380955.1:n.1877+58_1877+96delinsCCAGCAGCCGGGCTCACTCG...
ENST00000475170.5:n.1277+58_1277+96delinsCCAGCAGCCGGGCTCACTCGGGGACCCCAGTGAGCACCT
ENST00000498666.5:n.3933+58_3933+96delinsCCAGCAGCCGGGCTCACTCGGGGACCCCAGTGAGCACCT
ENST00000523323.5:c.*1704+58_*1704+96delinsCCAGCAGCCGGGCTCACTCGGGGACCCCAGTGAGCACCT	ENSP00000427732.1:n.*1704+58_*1704+96delinsCCAGCAGCCGGGCTCACT...
ENST00000610622.4:c.*568+58_*568+96delinsCCAGCAGCCGGGCTCACTCGGGGACCCCAGTGAGCACCT	ENSP00000480700.1:n.*568+58_*568+96delinsCCAGCAGCCGGGCTCACTCG...
NM_000211.4:c.1877+58_1877+96delinsCCAGCAGCCGGGCTCACTCGGGGACCCCAGTGAGCACCT	NP_000202.3:n.1877+58_1877+96delinsCCAGCAGCCGGGCTCACTCGGGGACC...
NM_001127491.2:c.1877+58_1877+96delinsCCAGCAGCCGGGCTCACTCGGGGACCCCAGTGAGCACCT	NP_001120963.2:n.1877+58_1877+96delinsCCAGCAGCCGGGCTCACTCGGGG...
NM_001303238.1:c.1670+58_1670+96delinsCCAGCAGCCGGGCTCACTCGGGGACCCCAGTGAGCACCT	NP_001290167.1:n.1670+58_1670+96delinsCCAGCAGCCGGGCTCACTCGGGG...
XM_006724001.1:c.1670+58_1670+96delinsCCAGCAGCCGGGCTCACTCGGGGACCCCAGTGAGCACCT	XP_006724064.1:n.1670+58_1670+96delinsCCAGCAGCCGGGCTCACTCGGGG...
XM_006724001.2:c.1670+58_1670+96delinsCCAGCAGCCGGGCTCACTCGGGGACCCCAGTGAGCACCT	XP_006724064.1:n.1670+58_1670+96delinsCCAGCAGCCGGGCTCACTCGGGG...
NM_000211.5:c.1877+58_1877+96delinsCCAGCAGCCGGGCTCACTCGGGGACCCCAGTGAGCACCT MANE Select	NP_000202.3:n.1877+58_1877+96delinsCCAGCAGCCGGGCTCACTCGGGGACC...
NM_001127491.3:c.1877+58_1877+96delinsCCAGCAGCCGGGCTCACTCGGGGACCCCAGTGAGCACCT	NP_001120963.2:n.1877+58_1877+96delinsCCAGCAGCCGGGCTCACTCGGGG...
NM_001303238.2:c.1670+58_1670+96delinsCCAGCAGCCGGGCTCACTCGGGGACCCCAGTGAGCACCT	NP_001290167.1:n.1670+58_1670+96delinsCCAGCAGCCGGGCTCACTCGGGG...