Canonical Allele Identifier: CA2391880200

Gene: ITGB2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44901540A= , CM000683.2:g.44901540A=	GRCh38
NC_000021.8:g.46321455A= , CM000683.1:g.46321455A=	GRCh37
NC_000021.7:g.45145883A=	NCBI36
NG_007270.2:g.32299T= , LRG_76:g.32299T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302347.10:c.693T=	ENSP00000303242.6:p.Asp231=
ENST00000652462.1:c.693T= MANE Select	ENSP00000498780.1:p.Asp231=
ENST00000302347.9:c.693T=	ENSP00000303242.5:p.Asp231=
ENST00000320216.10:c.666T=	ENSP00000317697.6:p.Asp222=
ENST00000355153.8:c.693T=	ENSP00000347279.4:p.Asp231=
ENST00000397850.6:c.693T=	ENSP00000380948.2:p.Asp231=
ENST00000397852.5:c.693T=	ENSP00000380950.1:p.Asp231=
ENST00000397854.7:c.522T=	ENSP00000380952.3:p.Asp174=
ENST00000397857.5:c.693T=	ENSP00000380955.1:p.Asp231=
ENST00000498666.5:n.836T=
ENST00000523323.5:c.*520T=	ENSP00000427732.1:n.*520T=
ENST00000610622.4:c.522T=	ENSP00000480700.1:p.Asp174=
NM_000211.4:c.693T=	NP_000202.3:p.Asp231=
NM_001127491.2:c.693T=	NP_001120963.2:p.Asp231=
NM_001303238.1:c.486T=	NP_001290167.1:p.Asp162=
XM_006724001.1:c.486T=	XP_006724064.1:p.Asp162=
XM_006724001.2:c.486T=	XP_006724064.1:p.Asp162=
NM_000211.5:c.693T= MANE Select	NP_000202.3:p.Asp231=
NM_001127491.3:c.693T=	NP_001120963.2:p.Asp231=
NM_001303238.2:c.486T=	NP_001290167.1:p.Asp162=