Canonical Allele Identifier: CA2818060533

Gene: ITGB2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44893046_44893052del , CM000683.2:g.44893046_44893052del	GRCh38
NC_000021.8:g.46312961_46312967del , CM000683.1:g.46312961_46312967del	GRCh37
NC_000021.7:g.45137389_45137395del	NCBI36
NG_007270.2:g.40787_40793del , LRG_76:g.40787_40793del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302347.10:c.1296+352_1296+358del	ENSP00000303242.6:n.1296+352_1296+358del
ENST00000652462.1:c.1224+352_1224+358del MANE Select	ENSP00000498780.1:n.1224+352_1224+358del
ENST00000302347.9:c.1224+352_1224+358del	ENSP00000303242.5:n.1224+352_1224+358del
ENST00000355153.8:c.1224+352_1224+358del	ENSP00000347279.4:n.1224+352_1224+358del
ENST00000397850.6:c.1224+352_1224+358del	ENSP00000380948.2:n.1224+352_1224+358del
ENST00000397852.5:c.1224+352_1224+358del	ENSP00000380950.1:n.1224+352_1224+358del
ENST00000397854.7:c.1053+352_1053+358del	ENSP00000380952.3:n.1053+352_1053+358del
ENST00000397857.5:c.1224+352_1224+358del	ENSP00000380955.1:n.1224+352_1224+358del
ENST00000475170.5:n.624+352_624+358del
ENST00000498666.5:n.3145_3151del
ENST00000523323.5:c.*1051+352_*1051+358del	ENSP00000427732.1:n.*1051+352_*1051+358del
ENST00000610622.4:c.1053+352_1053+358del	ENSP00000480700.1:n.1053+352_1053+358del
NM_000211.4:c.1224+352_1224+358del	NP_000202.3:n.1224+352_1224+358del
NM_001127491.2:c.1224+352_1224+358del	NP_001120963.2:n.1224+352_1224+358del
NM_001303238.1:c.1017+352_1017+358del	NP_001290167.1:n.1017+352_1017+358del
XM_006724001.1:c.1017+352_1017+358del	XP_006724064.1:n.1017+352_1017+358del
XM_006724001.2:c.1017+352_1017+358del	XP_006724064.1:n.1017+352_1017+358del
NM_000211.5:c.1224+352_1224+358del MANE Select	NP_000202.3:n.1224+352_1224+358del
NM_001127491.3:c.1224+352_1224+358del	NP_001120963.2:n.1224+352_1224+358del
NM_001303238.2:c.1017+352_1017+358del	NP_001290167.1:n.1017+352_1017+358del