Canonical Allele Identifier: CA2391876007

Gene: ITGB2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44893722C= , CM000683.2:g.44893722C=	GRCh38
NC_000021.8:g.46313637C= , CM000683.1:g.46313637C=	GRCh37
NC_000021.7:g.45138065C=	NCBI36
NG_007270.2:g.40117G= , LRG_76:g.40117G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302347.10:c.1156-178G=	ENSP00000303242.6:n.1156-178G=
ENST00000652462.1:c.1084-178G= MANE Select	ENSP00000498780.1:n.1084-178G=
ENST00000302347.9:c.1084-178G=	ENSP00000303242.5:n.1084-178G=
ENST00000355153.8:c.1084-178G=	ENSP00000347279.4:n.1084-178G=
ENST00000397850.6:c.1084-178G=	ENSP00000380948.2:n.1084-178G=
ENST00000397852.5:c.1084-178G=	ENSP00000380950.1:n.1084-178G=
ENST00000397854.7:c.913-178G=	ENSP00000380952.3:n.913-178G=
ENST00000397857.5:c.1084-178G=	ENSP00000380955.1:n.1084-178G=
ENST00000475170.5:n.306G=
ENST00000498666.5:n.2475G=
ENST00000523323.5:c.*911-178G=	ENSP00000427732.1:n.*911-178G=
ENST00000610622.4:c.913-178G=	ENSP00000480700.1:n.913-178G=
NM_000211.4:c.1084-178G=	NP_000202.3:n.1084-178G=
NM_001127491.2:c.1084-178G=	NP_001120963.2:n.1084-178G=
NM_001303238.1:c.877-178G=	NP_001290167.1:n.877-178G=
XM_006724001.1:c.877-178G=	XP_006724064.1:n.877-178G=
XM_006724001.2:c.877-178G=	XP_006724064.1:n.877-178G=
NM_000211.5:c.1084-178G= MANE Select	NP_000202.3:n.1084-178G=
NM_001127491.3:c.1084-178G=	NP_001120963.2:n.1084-178G=
NM_001303238.2:c.877-178G=	NP_001290167.1:n.877-178G=