Canonical Allele Identifier: CA2391872391

Gene: ITGB2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44886742C= , CM000683.2:g.44886742C=	GRCh38
NC_000021.8:g.46306657C= , CM000683.1:g.46306657C=	GRCh37
NC_000021.7:g.45131085C=	NCBI36
NG_007270.2:g.47097G= , LRG_76:g.47097G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696946.1:n.1448G=
ENST00000302347.10:c.2313G=	ENSP00000303242.6:p.Trp771=
ENST00000652462.1:c.2241G= MANE Select	ENSP00000498780.1:p.Trp747=
ENST00000302347.9:c.2241G=	ENSP00000303242.5:p.Trp747=
ENST00000355153.8:c.2241G=	ENSP00000347279.4:p.Trp747=
ENST00000397850.6:c.2241G=	ENSP00000380948.2:p.Trp747=
ENST00000397852.5:c.2241G=	ENSP00000380950.1:p.Trp747=
ENST00000397854.7:c.2070G=	ENSP00000380952.3:p.Trp690=
ENST00000397857.5:c.2241G=	ENSP00000380955.1:p.Trp747=
ENST00000475170.5:n.1641G=
ENST00000479202.5:n.600G=
ENST00000498666.5:n.4297G=
ENST00000523323.5:c.*2068G=	ENSP00000427732.1:n.*2068G=
ENST00000610622.4:c.*932G=	ENSP00000480700.1:n.*932G=
NM_000211.4:c.2241G=	NP_000202.3:p.Trp747=
NM_001127491.2:c.2241G=	NP_001120963.2:p.Trp747=
NM_001303238.1:c.2034G=	NP_001290167.1:p.Trp678=
XM_006724001.1:c.2034G=	XP_006724064.1:p.Trp678=
XM_006724001.2:c.2034G=	XP_006724064.1:p.Trp678=
NM_000211.5:c.2241G= MANE Select	NP_000202.3:p.Trp747=
NM_001127491.3:c.2241G=	NP_001120963.2:p.Trp747=
NM_001303238.2:c.2034G=	NP_001290167.1:p.Trp678=