Canonical Allele Identifier: CA2244514007

Gene: ARRB2

Linked Data

• dbSNP Id: rs1597468281

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4710639C>G , CM000679.2:g.4710639C>G	GRCh38
NC_000017.10:g.4613934C>G , CM000679.1:g.4613934C>G	GRCh37
NC_000017.9:g.4560683C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269260.7:c.-83C>G MANE Select	ENSP00000269260.2:n.-83C>G
ENST00000269260.6:c.-83C>G	ENSP00000269260.2:n.-83C>G
ENST00000346341.6:c.-83C>G	ENSP00000341895.2:n.-83C>G
ENST00000570718.5:n.8C>G
ENST00000570739.5:n.8C>G
ENST00000574502.5:c.-83C>G	ENSP00000458371.1:n.-83C>G
ENST00000574954.5:c.-628C>G	ENSP00000466344.1:n.-628C>G
NM_001257328.1:c.-83C>G	NP_001244257.1:n.-83C>G
NM_001257329.1:c.-83C>G	NP_001244258.1:n.-83C>G
NM_001257330.1:c.-83C>G	NP_001244259.1:n.-83C>G
NM_001257331.1:c.-83C>G	NP_001244260.1:n.-83C>G
NM_004313.3:c.-83C>G	NP_004304.1:n.-83C>G
NM_199004.1:c.-83C>G	NP_945355.1:n.-83C>G
NR_047516.1:n.146C>G
XM_006721520.1:c.-583C>G	XP_006721583.1:n.-583C>G
NM_001330064.1:c.-583C>G	NP_001316993.1:n.-583C>G
XM_024450751.1:c.-83C>G	XP_024306519.1:n.-83C>G
XM_024450752.1:c.-628C>G	XP_024306520.1:n.-628C>G
XM_024450753.1:c.-583C>G	XP_024306521.1:n.-583C>G
XR_002958006.1:n.10C>G
XR_002958007.1:n.10C>G
NM_004313.4:c.-83C>G MANE Select	NP_004304.1:n.-83C>G
NM_001257328.2:c.-83C>G	NP_001244257.1:n.-83C>G
NM_001257329.2:c.-83C>G	NP_001244258.1:n.-83C>G
NM_001257330.2:c.-83C>G	NP_001244259.1:n.-83C>G
NM_001257331.2:c.-83C>G	NP_001244260.1:n.-83C>G
NM_001330064.2:c.-583C>G	NP_001316993.1:n.-583C>G
NM_199004.2:c.-83C>G	NP_945355.1:n.-83C>G
NR_047516.2:n.8C>G