Canonical Allele Identifier: CA2391890442

Gene: ITGB2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44920928A= , CM000683.2:g.44920928A=	GRCh38
NC_000021.8:g.46340843A= , CM000683.1:g.46340843A=	GRCh37
NC_000021.7:g.45165271A=	NCBI36
NG_007270.2:g.12911T= , LRG_76:g.12911T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000211.4:c.-111T=	NP_000202.3:n.-111T=
NM_001127491.2:c.-4+7726T=	NP_001120963.2:n.-4+7726T=
NM_001127491.3:c.-4+7726T=	NP_001120963.2:n.-4+7726T=
NM_001303238.1:c.-361T=	NP_001290167.1:n.-361T=
ENST00000302347.9:c.-111T=	ENSP00000303242.5:n.-111T=
ENST00000355153.8:c.-4+7726T=	ENSP00000347279.4:n.-4+7726T=
ENST00000397850.6:c.-111T=	ENSP00000380948.2:n.-111T=
ENST00000498666.5:n.33T=
ENST00000517563.5:c.-111T=	ENSP00000428413.1:n.-111T=
ENST00000517819.5:c.-111T=	ENSP00000428870.1:n.-111T=
ENST00000521987.1:n.5T=
ENST00000521995.1:c.-111T=	ENSP00000429683.1:n.-111T=
ENST00000522688.5:c.-443T=	ENSP00000428125.1:n.-443T=
XM_006724001.1:c.-443T=	XP_006724064.1:n.-443T=
XM_006724001.2:c.-443T=	XP_006724064.1:n.-443T=