Canonical Allele Identifier: CA2391872399

Gene: ITGB2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44886774G= , CM000683.2:g.44886774G=	GRCh38
NC_000021.8:g.46306689G= , CM000683.1:g.46306689G=	GRCh37
NC_000021.7:g.45131117G=	NCBI36
NG_007270.2:g.47065C= , LRG_76:g.47065C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696946.1:n.1416C=
ENST00000302347.10:c.2281C=	ENSP00000303242.6:p.Arg761=
ENST00000652462.1:c.2209C= MANE Select	ENSP00000498780.1:p.Arg737=
ENST00000302347.9:c.2209C=	ENSP00000303242.5:p.Arg737=
ENST00000355153.8:c.2209C=	ENSP00000347279.4:p.Arg737=
ENST00000397850.6:c.2209C=	ENSP00000380948.2:p.Arg737=
ENST00000397852.5:c.2209C=	ENSP00000380950.1:p.Arg737=
ENST00000397854.7:c.2038C=	ENSP00000380952.3:p.Arg680=
ENST00000397857.5:c.2209C=	ENSP00000380955.1:p.Arg737=
ENST00000475170.5:n.1609C=
ENST00000479202.5:n.568C=
ENST00000498666.5:n.4265C=
ENST00000523323.5:c.*2036C=	ENSP00000427732.1:n.*2036C=
ENST00000610622.4:c.*900C=	ENSP00000480700.1:n.*900C=
NM_000211.4:c.2209C=	NP_000202.3:p.Arg737=
NM_001127491.2:c.2209C=	NP_001120963.2:p.Arg737=
NM_001303238.1:c.2002C=	NP_001290167.1:p.Arg668=
XM_006724001.1:c.2002C=	XP_006724064.1:p.Arg668=
XM_006724001.2:c.2002C=	XP_006724064.1:p.Arg668=
NM_000211.5:c.2209C= MANE Select	NP_000202.3:p.Arg737=
NM_001127491.3:c.2209C=	NP_001120963.2:p.Arg737=
NM_001303238.2:c.2002C=	NP_001290167.1:p.Arg668=