Canonical Allele Identifier: CA2391873845

Gene: ITGB2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44889454C= , CM000683.2:g.44889454C=	GRCh38
NC_000021.8:g.46309369C= , CM000683.1:g.46309369C=	GRCh37
NC_000021.7:g.45133797C=	NCBI36
NG_007270.2:g.44385G= , LRG_76:g.44385G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696946.1:n.906G=
ENST00000302347.10:c.1771G=	ENSP00000303242.6:p.Gly591=
ENST00000652462.1:c.1699G= MANE Select	ENSP00000498780.1:p.Gly567=
ENST00000302347.9:c.1699G=	ENSP00000303242.5:p.Gly567=
ENST00000355153.8:c.1699G=	ENSP00000347279.4:p.Gly567=
ENST00000397850.6:c.1699G=	ENSP00000380948.2:p.Gly567=
ENST00000397852.5:c.1699G=	ENSP00000380950.1:p.Gly567=
ENST00000397854.7:c.1528G=	ENSP00000380952.3:p.Gly510=
ENST00000397857.5:c.1699G=	ENSP00000380955.1:p.Gly567=
ENST00000475170.5:n.1099G=
ENST00000498666.5:n.3755G=
ENST00000523323.5:c.*1526G=	ENSP00000427732.1:n.*1526G=
ENST00000610622.4:c.*390G=	ENSP00000480700.1:n.*390G=
NM_000211.4:c.1699G=	NP_000202.3:p.Gly567=
NM_001127491.2:c.1699G=	NP_001120963.2:p.Gly567=
NM_001303238.1:c.1492G=	NP_001290167.1:p.Gly498=
XM_006724001.1:c.1492G=	XP_006724064.1:p.Gly498=
XM_006724001.2:c.1492G=	XP_006724064.1:p.Gly498=
NM_000211.5:c.1699G= MANE Select	NP_000202.3:p.Gly567=
NM_001127491.3:c.1699G=	NP_001120963.2:p.Gly567=
NM_001303238.2:c.1492G=	NP_001290167.1:p.Gly498=