Canonical Allele Identifier: CA2391872354

Gene: ITGB2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44886685_44886708delinsTGTGGGACGCACGTGCCCCTCTGC , CM000683.2:g.44886685_44886708delinsTGTGGGACGCACGTGCCCCTCTGC	GRCh38
NC_000021.8:g.46306600_46306623delinsTGTGGGACGCACGTGCCCCTCTGC , CM000683.1:g.46306600_46306623delinsTGTGGGACGCACGTGCCCCTCTGC	GRCh37
NC_000021.7:g.45131028_45131051delinsTGTGGGACGCACGTGCCCCTCTGC	NCBI36
NG_007270.2:g.47131_47154delinsGCAGAGGGGCACGTGCGTCCCACA , LRG_76:g.47131_47154delinsGCAGAGGGGCACGTGCGTCCCACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696946.1:n.1454+28_1454+51delinsGCAGAGGGGCACGTGCGTCCCACA
ENST00000302347.10:c.2319+28_2319+51delinsGCAGAGGGGCACGTGCGTCCCACA	ENSP00000303242.6:n.2319+28_2319+51delinsGCAGAGGGGCACGTGCGTCC...
ENST00000652462.1:c.2247+28_2247+51delinsGCAGAGGGGCACGTGCGTCCCACA MANE Select	ENSP00000498780.1:n.2247+28_2247+51delinsGCAGAGGGGCACGTGCGTCC...
ENST00000302347.9:c.2247+28_2247+51delinsGCAGAGGGGCACGTGCGTCCCACA	ENSP00000303242.5:n.2247+28_2247+51delinsGCAGAGGGGCACGTGCGTCC...
ENST00000355153.8:c.2247+28_2247+51delinsGCAGAGGGGCACGTGCGTCCCACA	ENSP00000347279.4:n.2247+28_2247+51delinsGCAGAGGGGCACGTGCGTCC...
ENST00000397850.6:c.2247+28_2247+51delinsGCAGAGGGGCACGTGCGTCCCACA	ENSP00000380948.2:n.2247+28_2247+51delinsGCAGAGGGGCACGTGCGTCC...
ENST00000397852.5:c.2247+28_2247+51delinsGCAGAGGGGCACGTGCGTCCCACA	ENSP00000380950.1:n.2247+28_2247+51delinsGCAGAGGGGCACGTGCGTCC...
ENST00000397854.7:c.2076+28_2076+51delinsGCAGAGGGGCACGTGCGTCCCACA	ENSP00000380952.3:n.2076+28_2076+51delinsGCAGAGGGGCACGTGCGTCC...
ENST00000397857.5:c.2247+28_2247+51delinsGCAGAGGGGCACGTGCGTCCCACA	ENSP00000380955.1:n.2247+28_2247+51delinsGCAGAGGGGCACGTGCGTCC...
ENST00000475170.5:n.1647+28_1647+51delinsGCAGAGGGGCACGTGCGTCCCACA
ENST00000479202.5:n.606+28_606+51delinsGCAGAGGGGCACGTGCGTCCCACA
ENST00000498666.5:n.4303+28_4303+51delinsGCAGAGGGGCACGTGCGTCCCACA
ENST00000523323.5:c.*2074+28_*2074+51delinsGCAGAGGGGCACGTGCGTCCCACA	ENSP00000427732.1:n.*2074+28_*2074+51delinsGCAGAGGGGCACGTGCGT...
ENST00000610622.4:c.*938+28_*938+51delinsGCAGAGGGGCACGTGCGTCCCACA	ENSP00000480700.1:n.*938+28_*938+51delinsGCAGAGGGGCACGTGCGTCC...
NM_000211.4:c.2247+28_2247+51delinsGCAGAGGGGCACGTGCGTCCCACA	NP_000202.3:n.2247+28_2247+51delinsGCAGAGGGGCACGTGCGTCCCACA
NM_001127491.2:c.2247+28_2247+51delinsGCAGAGGGGCACGTGCGTCCCACA	NP_001120963.2:n.2247+28_2247+51delinsGCAGAGGGGCACGTGCGTCCCAC...
NM_001303238.1:c.2040+28_2040+51delinsGCAGAGGGGCACGTGCGTCCCACA	NP_001290167.1:n.2040+28_2040+51delinsGCAGAGGGGCACGTGCGTCCCAC...
XM_006724001.1:c.2040+28_2040+51delinsGCAGAGGGGCACGTGCGTCCCACA	XP_006724064.1:n.2040+28_2040+51delinsGCAGAGGGGCACGTGCGTCCCAC...
XM_006724001.2:c.2040+28_2040+51delinsGCAGAGGGGCACGTGCGTCCCACA	XP_006724064.1:n.2040+28_2040+51delinsGCAGAGGGGCACGTGCGTCCCAC...
NM_000211.5:c.2247+28_2247+51delinsGCAGAGGGGCACGTGCGTCCCACA MANE Select	NP_000202.3:n.2247+28_2247+51delinsGCAGAGGGGCACGTGCGTCCCACA
NM_001127491.3:c.2247+28_2247+51delinsGCAGAGGGGCACGTGCGTCCCACA	NP_001120963.2:n.2247+28_2247+51delinsGCAGAGGGGCACGTGCGTCCCAC...
NM_001303238.2:c.2040+28_2040+51delinsGCAGAGGGGCACGTGCGTCCCACA	NP_001290167.1:n.2040+28_2040+51delinsGCAGAGGGGCACGTGCGTCCCAC...