Canonical Allele Identifier: CA2244514018

Gene: ARRB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4710661G= , CM000679.2:g.4710661G=	GRCh38
NC_000017.10:g.4613956G= , CM000679.1:g.4613956G=	GRCh37
NC_000017.9:g.4560705G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269260.7:c.-61G= MANE Select	ENSP00000269260.2:n.-61G=
ENST00000269260.6:c.-61G=	ENSP00000269260.2:n.-61G=
ENST00000346341.6:c.-61G=	ENSP00000341895.2:n.-61G=
ENST00000570718.5:n.30G=
ENST00000570739.5:n.30G=
ENST00000572457.5:c.-545G=	ENSP00000465296.1:n.-545G=
ENST00000574502.5:c.-61G=	ENSP00000458371.1:n.-61G=
ENST00000574888.5:n.7G=
ENST00000574954.5:c.-606G=	ENSP00000466344.1:n.-606G=
ENST00000575131.5:n.1G=
NM_001257328.1:c.-61G=	NP_001244257.1:n.-61G=
NM_001257329.1:c.-61G=	NP_001244258.1:n.-61G=
NM_001257330.1:c.-61G=	NP_001244259.1:n.-61G=
NM_001257331.1:c.-61G=	NP_001244260.1:n.-61G=
NM_004313.3:c.-61G=	NP_004304.1:n.-61G=
NM_199004.1:c.-61G=	NP_945355.1:n.-61G=
NR_047516.1:n.168G=
XM_006721520.1:c.-561G=	XP_006721583.1:n.-561G=
NM_001330064.1:c.-561G=	NP_001316993.1:n.-561G=
XM_024450751.1:c.-61G=	XP_024306519.1:n.-61G=
XM_024450752.1:c.-606G=	XP_024306520.1:n.-606G=
XM_024450753.1:c.-561G=	XP_024306521.1:n.-561G=
XR_002958006.1:n.32G=
XR_002958007.1:n.32G=
NM_004313.4:c.-61G= MANE Select	NP_004304.1:n.-61G=
NM_001257328.2:c.-61G=	NP_001244257.1:n.-61G=
NM_001257329.2:c.-61G=	NP_001244258.1:n.-61G=
NM_001257330.2:c.-61G=	NP_001244259.1:n.-61G=
NM_001257331.2:c.-61G=	NP_001244260.1:n.-61G=
NM_001330064.2:c.-561G=	NP_001316993.1:n.-561G=
NM_199004.2:c.-61G=	NP_945355.1:n.-61G=
NR_047516.2:n.30G=