Canonical Allele Identifier: CA2391875875

Gene: ITGB2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44893422G= , CM000683.2:g.44893422G=	GRCh38
NC_000021.8:g.46313337G= , CM000683.1:g.46313337G=	GRCh37
NC_000021.7:g.45137765G=	NCBI36
NG_007270.2:g.40417C= , LRG_76:g.40417C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302347.10:c.1278C=	ENSP00000303242.6:p.Gly426=
ENST00000652462.1:c.1206C= MANE Select	ENSP00000498780.1:p.Gly402=
ENST00000302347.9:c.1206C=	ENSP00000303242.5:p.Gly402=
ENST00000355153.8:c.1206C=	ENSP00000347279.4:p.Gly402=
ENST00000397850.6:c.1206C=	ENSP00000380948.2:p.Gly402=
ENST00000397852.5:c.1206C=	ENSP00000380950.1:p.Gly402=
ENST00000397854.7:c.1035C=	ENSP00000380952.3:p.Gly345=
ENST00000397857.5:c.1206C=	ENSP00000380955.1:p.Gly402=
ENST00000475170.5:n.606C=
ENST00000498666.5:n.2775C=
ENST00000523323.5:c.*1033C=	ENSP00000427732.1:n.*1033C=
ENST00000610622.4:c.1035C=	ENSP00000480700.1:p.Gly345=
NM_000211.4:c.1206C=	NP_000202.3:p.Gly402=
NM_001127491.2:c.1206C=	NP_001120963.2:p.Gly402=
NM_001303238.1:c.999C=	NP_001290167.1:p.Gly333=
XM_006724001.1:c.999C=	XP_006724064.1:p.Gly333=
XM_006724001.2:c.999C=	XP_006724064.1:p.Gly333=
NM_000211.5:c.1206C= MANE Select	NP_000202.3:p.Gly402=
NM_001127491.3:c.1206C=	NP_001120963.2:p.Gly402=
NM_001303238.2:c.999C=	NP_001290167.1:p.Gly333=