Canonical Allele Identifier: CA2391872411

Gene: ITGB2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44886801G= , CM000683.2:g.44886801G=	GRCh38
NC_000021.8:g.46306716G= , CM000683.1:g.46306716G=	GRCh37
NC_000021.7:g.45131144G=	NCBI36
NG_007270.2:g.47038C= , LRG_76:g.47038C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696946.1:n.1389C=
ENST00000302347.10:c.2254C=	ENSP00000303242.6:p.His752=
ENST00000652462.1:c.2182C= MANE Select	ENSP00000498780.1:p.His728=
ENST00000302347.9:c.2182C=	ENSP00000303242.5:p.His728=
ENST00000355153.8:c.2182C=	ENSP00000347279.4:p.His728=
ENST00000397850.6:c.2182C=	ENSP00000380948.2:p.His728=
ENST00000397852.5:c.2182C=	ENSP00000380950.1:p.His728=
ENST00000397854.7:c.2011C=	ENSP00000380952.3:p.His671=
ENST00000397857.5:c.2182C=	ENSP00000380955.1:p.His728=
ENST00000475170.5:n.1582C=
ENST00000479202.5:n.541C=
ENST00000498666.5:n.4238C=
ENST00000523323.5:c.*2009C=	ENSP00000427732.1:n.*2009C=
ENST00000610622.4:c.*873C=	ENSP00000480700.1:n.*873C=
NM_000211.4:c.2182C=	NP_000202.3:p.His728=
NM_001127491.2:c.2182C=	NP_001120963.2:p.His728=
NM_001303238.1:c.1975C=	NP_001290167.1:p.His659=
XM_006724001.1:c.1975C=	XP_006724064.1:p.His659=
XM_006724001.2:c.1975C=	XP_006724064.1:p.His659=
NM_000211.5:c.2182C= MANE Select	NP_000202.3:p.His728=
NM_001127491.3:c.2182C=	NP_001120963.2:p.His728=
NM_001303238.2:c.1975C=	NP_001290167.1:p.His659=