Canonical Allele Identifier: CA2654866557

Gene: ITGB2

Linked Data

• gnomAD v4: 21-44893052-G-GCGAGTGTTTCTGTTGTCCTGGCCCTGCCTGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44893053_44893054insGAGTGTTTCTGTTGTCCTGGCCCTGCCTGGCC , CM000683.2:g.44893053_44893054insGAGTGTTTCTGTTGTCCTGGCCCTGCCTGGCC	GRCh38
NC_000021.8:g.46312968_46312969insGAGTGTTTCTGTTGTCCTGGCCCTGCCTGGCC , CM000683.1:g.46312968_46312969insGAGTGTTTCTGTTGTCCTGGCCCTGCCTGGCC	GRCh37
NC_000021.7:g.45137396_45137397insGAGTGTTTCTGTTGTCCTGGCCCTGCCTGGCC	NCBI36
NG_007270.2:g.40786_40787insGCCAGGCAGGGCCAGGACAACAGAAACACTCG , LRG_76:g.40786_40787insGCCAGGCAGGGCCAGGACAACAGAAACACTCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302347.10:c.1296+351_1296+352insGCCAGGCAGGGCCAGGACAACAGAAACACTCG	ENSP00000303242.6:n.1296+351_1296+352insGCCAGGCAGGGCCAGGACAAC...
ENST00000652462.1:c.1224+351_1224+352insGCCAGGCAGGGCCAGGACAACAGAAACACTCG MANE Select	ENSP00000498780.1:n.1224+351_1224+352insGCCAGGCAGGGCCAGGACAAC...
ENST00000302347.9:c.1224+351_1224+352insGCCAGGCAGGGCCAGGACAACAGAAACACTCG	ENSP00000303242.5:n.1224+351_1224+352insGCCAGGCAGGGCCAGGACAAC...
ENST00000355153.8:c.1224+351_1224+352insGCCAGGCAGGGCCAGGACAACAGAAACACTCG	ENSP00000347279.4:n.1224+351_1224+352insGCCAGGCAGGGCCAGGACAAC...
ENST00000397850.6:c.1224+351_1224+352insGCCAGGCAGGGCCAGGACAACAGAAACACTCG	ENSP00000380948.2:n.1224+351_1224+352insGCCAGGCAGGGCCAGGACAAC...
ENST00000397852.5:c.1224+351_1224+352insGCCAGGCAGGGCCAGGACAACAGAAACACTCG	ENSP00000380950.1:n.1224+351_1224+352insGCCAGGCAGGGCCAGGACAAC...
ENST00000397854.7:c.1053+351_1053+352insGCCAGGCAGGGCCAGGACAACAGAAACACTCG	ENSP00000380952.3:n.1053+351_1053+352insGCCAGGCAGGGCCAGGACAAC...
ENST00000397857.5:c.1224+351_1224+352insGCCAGGCAGGGCCAGGACAACAGAAACACTCG	ENSP00000380955.1:n.1224+351_1224+352insGCCAGGCAGGGCCAGGACAAC...
ENST00000475170.5:n.624+351_624+352insGCCAGGCAGGGCCAGGACAACAGAAACACTCG
ENST00000498666.5:n.3144_3145insGCCAGGCAGGGCCAGGACAACAGAAACACTCG
ENST00000523323.5:c.*1051+351_*1051+352insGCCAGGCAGGGCCAGGACAACAGAAACACTCG	ENSP00000427732.1:n.*1051+351_*1051+352insGCCAGGCAGGGCCAGGACA...
ENST00000610622.4:c.1053+351_1053+352insGCCAGGCAGGGCCAGGACAACAGAAACACTCG	ENSP00000480700.1:n.1053+351_1053+352insGCCAGGCAGGGCCAGGACAAC...
NM_000211.4:c.1224+351_1224+352insGCCAGGCAGGGCCAGGACAACAGAAACACTCG	NP_000202.3:n.1224+351_1224+352insGCCAGGCAGGGCCAGGACAACAGAAAC...
NM_001127491.2:c.1224+351_1224+352insGCCAGGCAGGGCCAGGACAACAGAAACACTCG	NP_001120963.2:n.1224+351_1224+352insGCCAGGCAGGGCCAGGACAACAGA...
NM_001303238.1:c.1017+351_1017+352insGCCAGGCAGGGCCAGGACAACAGAAACACTCG	NP_001290167.1:n.1017+351_1017+352insGCCAGGCAGGGCCAGGACAACAGA...
XM_006724001.1:c.1017+351_1017+352insGCCAGGCAGGGCCAGGACAACAGAAACACTCG	XP_006724064.1:n.1017+351_1017+352insGCCAGGCAGGGCCAGGACAACAGA...
XM_006724001.2:c.1017+351_1017+352insGCCAGGCAGGGCCAGGACAACAGAAACACTCG	XP_006724064.1:n.1017+351_1017+352insGCCAGGCAGGGCCAGGACAACAGA...
NM_000211.5:c.1224+351_1224+352insGCCAGGCAGGGCCAGGACAACAGAAACACTCG MANE Select	NP_000202.3:n.1224+351_1224+352insGCCAGGCAGGGCCAGGACAACAGAAAC...
NM_001127491.3:c.1224+351_1224+352insGCCAGGCAGGGCCAGGACAACAGAAACACTCG	NP_001120963.2:n.1224+351_1224+352insGCCAGGCAGGGCCAGGACAACAGA...
NM_001303238.2:c.1017+351_1017+352insGCCAGGCAGGGCCAGGACAACAGAAACACTCG	NP_001290167.1:n.1017+351_1017+352insGCCAGGCAGGGCCAGGACAACAGA...