Canonical Allele Identifier: CA2244519353

Gene: ARRB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4719359C= , CM000679.2:g.4719359C=	GRCh38
NC_000017.10:g.4622654C= , CM000679.1:g.4622654C=	GRCh37
NC_000017.9:g.4569403C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269260.7:c.856C= MANE Select	ENSP00000269260.2:p.Arg286=
ENST00000269260.6:c.856C=	ENSP00000269260.2:p.Arg286=
ENST00000346341.6:c.811C=	ENSP00000341895.2:p.Arg271=
ENST00000381488.10:c.811C=	ENSP00000370898.6:p.Arg271=
ENST00000412477.7:c.919C=	ENSP00000403701.3:p.Arg307=
ENST00000571206.1:c.280C=	ENSP00000460607.1:p.Arg94=
ENST00000571428.5:c.280C=	ENSP00000465877.1:p.Arg94=
ENST00000572457.5:c.280C=	ENSP00000465296.1:p.Arg94=
ENST00000574502.5:c.*334C=	ENSP00000458371.1:n.*334C=
ENST00000574954.5:c.280C=	ENSP00000466344.1:p.Arg94=
ENST00000575877.5:c.786+70C=	ENSP00000466857.1:n.786+70C=
ENST00000576235.1:c.738C=	ENSP00000460879.1:n.738C=
NM_001257328.1:c.919C=	NP_001244257.1:p.Arg307=
NM_001257329.1:c.786+70C=	NP_001244258.1:n.786+70C=
NM_001257330.1:c.856C=	NP_001244259.1:p.Arg286=
NM_001257331.1:c.811C=	NP_001244260.1:p.Arg271=
NM_004313.3:c.856C=	NP_004304.1:p.Arg286=
NM_199004.1:c.811C=	NP_945355.1:p.Arg271=
NR_047516.1:n.1053C=
XM_006721520.1:c.280C=	XP_006721583.1:p.Arg94=
XM_006721521.1:c.280C=	XP_006721584.1:p.Arg94=
XM_011523858.1:c.949C=	XP_011522160.1:p.Arg317=
XM_011523859.1:c.904C=	XP_011522161.1:p.Arg302=
NM_001330064.1:c.280C=	NP_001316993.1:p.Arg94=
XM_011523858.2:c.949C=	XP_011522160.1:p.Arg317=
XM_017024645.1:c.280C=	XP_016880134.1:p.Arg94=
XM_024450751.1:c.856C=	XP_024306519.1:p.Arg286=
XM_024450752.1:c.280C=	XP_024306520.1:p.Arg94=
XM_024450753.1:c.280C=	XP_024306521.1:p.Arg94=
XR_002958006.1:n.863C=
XR_002958007.1:n.863C=
NM_004313.4:c.856C= MANE Select	NP_004304.1:p.Arg286=
NM_001257328.2:c.919C=	NP_001244257.1:p.Arg307=
NM_001257329.2:c.786+70C=	NP_001244258.1:n.786+70C=
NM_001257330.2:c.856C=	NP_001244259.1:p.Arg286=
NM_001257331.2:c.811C=	NP_001244260.1:p.Arg271=
NM_001330064.2:c.280C=	NP_001316993.1:p.Arg94=
NM_199004.2:c.811C=	NP_945355.1:p.Arg271=
NR_047516.2:n.915C=