Canonical Allele Identifier: CA2654866855

Gene: ITGB2

Linked Data

• gnomAD v4: 21-44893310-C-CTAGCACAGGGCAGGAGCTG

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44893310_44893311insTAGCACAGGGCAGGAGCTG , CM000683.2:g.44893310_44893311insTAGCACAGGGCAGGAGCTG	GRCh38
NC_000021.8:g.46313225_46313226insTAGCACAGGGCAGGAGCTG , CM000683.1:g.46313225_46313226insTAGCACAGGGCAGGAGCTG	GRCh37
NC_000021.7:g.45137653_45137654insTAGCACAGGGCAGGAGCTG	NCBI36
NG_007270.2:g.40528_40529insCAGCTCCTGCCCTGTGCTA , LRG_76:g.40528_40529insCAGCTCCTGCCCTGTGCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302347.10:c.1296+93_1296+94insCAGCTCCTGCCCTGTGCTA	ENSP00000303242.6:n.1296+93_1296+94insCAGCTCCTGCCCTGTGCTA
ENST00000652462.1:c.1224+93_1224+94insCAGCTCCTGCCCTGTGCTA MANE Select	ENSP00000498780.1:n.1224+93_1224+94insCAGCTCCTGCCCTGTGCTA
ENST00000302347.9:c.1224+93_1224+94insCAGCTCCTGCCCTGTGCTA	ENSP00000303242.5:n.1224+93_1224+94insCAGCTCCTGCCCTGTGCTA
ENST00000355153.8:c.1224+93_1224+94insCAGCTCCTGCCCTGTGCTA	ENSP00000347279.4:n.1224+93_1224+94insCAGCTCCTGCCCTGTGCTA
ENST00000397850.6:c.1224+93_1224+94insCAGCTCCTGCCCTGTGCTA	ENSP00000380948.2:n.1224+93_1224+94insCAGCTCCTGCCCTGTGCTA
ENST00000397852.5:c.1224+93_1224+94insCAGCTCCTGCCCTGTGCTA	ENSP00000380950.1:n.1224+93_1224+94insCAGCTCCTGCCCTGTGCTA
ENST00000397854.7:c.1053+93_1053+94insCAGCTCCTGCCCTGTGCTA	ENSP00000380952.3:n.1053+93_1053+94insCAGCTCCTGCCCTGTGCTA
ENST00000397857.5:c.1224+93_1224+94insCAGCTCCTGCCCTGTGCTA	ENSP00000380955.1:n.1224+93_1224+94insCAGCTCCTGCCCTGTGCTA
ENST00000475170.5:n.624+93_624+94insCAGCTCCTGCCCTGTGCTA
ENST00000498666.5:n.2886_2887insCAGCTCCTGCCCTGTGCTA
ENST00000523323.5:c.*1051+93_*1051+94insCAGCTCCTGCCCTGTGCTA	ENSP00000427732.1:n.*1051+93_*1051+94insCAGCTCCTGCCCTGTGCTA
ENST00000610622.4:c.1053+93_1053+94insCAGCTCCTGCCCTGTGCTA	ENSP00000480700.1:n.1053+93_1053+94insCAGCTCCTGCCCTGTGCTA
NM_000211.4:c.1224+93_1224+94insCAGCTCCTGCCCTGTGCTA	NP_000202.3:n.1224+93_1224+94insCAGCTCCTGCCCTGTGCTA
NM_001127491.2:c.1224+93_1224+94insCAGCTCCTGCCCTGTGCTA	NP_001120963.2:n.1224+93_1224+94insCAGCTCCTGCCCTGTGCTA
NM_001303238.1:c.1017+93_1017+94insCAGCTCCTGCCCTGTGCTA	NP_001290167.1:n.1017+93_1017+94insCAGCTCCTGCCCTGTGCTA
XM_006724001.1:c.1017+93_1017+94insCAGCTCCTGCCCTGTGCTA	XP_006724064.1:n.1017+93_1017+94insCAGCTCCTGCCCTGTGCTA
XM_006724001.2:c.1017+93_1017+94insCAGCTCCTGCCCTGTGCTA	XP_006724064.1:n.1017+93_1017+94insCAGCTCCTGCCCTGTGCTA
NM_000211.5:c.1224+93_1224+94insCAGCTCCTGCCCTGTGCTA MANE Select	NP_000202.3:n.1224+93_1224+94insCAGCTCCTGCCCTGTGCTA
NM_001127491.3:c.1224+93_1224+94insCAGCTCCTGCCCTGTGCTA	NP_001120963.2:n.1224+93_1224+94insCAGCTCCTGCCCTGTGCTA
NM_001303238.2:c.1017+93_1017+94insCAGCTCCTGCCCTGTGCTA	NP_001290167.1:n.1017+93_1017+94insCAGCTCCTGCCCTGTGCTA