Canonical Allele Identifier: CA2391872409

Gene: ITGB2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44886798G= , CM000683.2:g.44886798G=	GRCh38
NC_000021.8:g.46306713G= , CM000683.1:g.46306713G=	GRCh37
NC_000021.7:g.45131141G=	NCBI36
NG_007270.2:g.47041C= , LRG_76:g.47041C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696946.1:n.1392C=
ENST00000302347.10:c.2257C=	ENSP00000303242.6:p.Leu753=
ENST00000652462.1:c.2185C= MANE Select	ENSP00000498780.1:p.Leu729=
ENST00000302347.9:c.2185C=	ENSP00000303242.5:p.Leu729=
ENST00000355153.8:c.2185C=	ENSP00000347279.4:p.Leu729=
ENST00000397850.6:c.2185C=	ENSP00000380948.2:p.Leu729=
ENST00000397852.5:c.2185C=	ENSP00000380950.1:p.Leu729=
ENST00000397854.7:c.2014C=	ENSP00000380952.3:p.Leu672=
ENST00000397857.5:c.2185C=	ENSP00000380955.1:p.Leu729=
ENST00000475170.5:n.1585C=
ENST00000479202.5:n.544C=
ENST00000498666.5:n.4241C=
ENST00000523323.5:c.*2012C=	ENSP00000427732.1:n.*2012C=
ENST00000610622.4:c.*876C=	ENSP00000480700.1:n.*876C=
NM_000211.4:c.2185C=	NP_000202.3:p.Leu729=
NM_001127491.2:c.2185C=	NP_001120963.2:p.Leu729=
NM_001303238.1:c.1978C=	NP_001290167.1:p.Leu660=
XM_006724001.1:c.1978C=	XP_006724064.1:p.Leu660=
XM_006724001.2:c.1978C=	XP_006724064.1:p.Leu660=
NM_000211.5:c.2185C= MANE Select	NP_000202.3:p.Leu729=
NM_001127491.3:c.2185C=	NP_001120963.2:p.Leu729=
NM_001303238.2:c.1978C=	NP_001290167.1:p.Leu660=