Canonical Allele Identifier: CA2635543318

Gene: ARRB2

Linked Data

• gnomAD v4: 17-4710678-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4710678C>A , CM000679.2:g.4710678C>A	GRCh38
NC_000017.10:g.4613973C>A , CM000679.1:g.4613973C>A	GRCh37
NC_000017.9:g.4560722C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269260.7:c.-44C>A MANE Select	ENSP00000269260.2:n.-44C>A
ENST00000269260.6:c.-44C>A	ENSP00000269260.2:n.-44C>A
ENST00000346341.6:c.-44C>A	ENSP00000341895.2:n.-44C>A
ENST00000570718.5:n.47C>A
ENST00000570739.5:n.47C>A
ENST00000572457.5:c.-528C>A	ENSP00000465296.1:n.-528C>A
ENST00000574502.5:c.-44C>A	ENSP00000458371.1:n.-44C>A
ENST00000574888.5:n.24C>A
ENST00000574954.5:c.-589C>A	ENSP00000466344.1:n.-589C>A
ENST00000575131.5:n.18C>A
NM_001257328.1:c.-44C>A	NP_001244257.1:n.-44C>A
NM_001257329.1:c.-44C>A	NP_001244258.1:n.-44C>A
NM_001257330.1:c.-44C>A	NP_001244259.1:n.-44C>A
NM_001257331.1:c.-44C>A	NP_001244260.1:n.-44C>A
NM_004313.3:c.-44C>A	NP_004304.1:n.-44C>A
NM_199004.1:c.-44C>A	NP_945355.1:n.-44C>A
NR_047516.1:n.185C>A
XM_006721520.1:c.-544C>A	XP_006721583.1:n.-544C>A
NM_001330064.1:c.-544C>A	NP_001316993.1:n.-544C>A
XM_024450751.1:c.-44C>A	XP_024306519.1:n.-44C>A
XM_024450752.1:c.-589C>A	XP_024306520.1:n.-589C>A
XM_024450753.1:c.-544C>A	XP_024306521.1:n.-544C>A
XR_002958006.1:n.49C>A
XR_002958007.1:n.49C>A
NM_004313.4:c.-44C>A MANE Select	NP_004304.1:n.-44C>A
NM_001257328.2:c.-44C>A	NP_001244257.1:n.-44C>A
NM_001257329.2:c.-44C>A	NP_001244258.1:n.-44C>A
NM_001257330.2:c.-44C>A	NP_001244259.1:n.-44C>A
NM_001257331.2:c.-44C>A	NP_001244260.1:n.-44C>A
NM_001330064.2:c.-544C>A	NP_001316993.1:n.-544C>A
NM_199004.2:c.-44C>A	NP_945355.1:n.-44C>A
NR_047516.2:n.47C>A