Canonical Allele Identifier: CA14369283

Gene: ARRB2

Linked Data

• dbSNP Id: rs3786047
• gnomAD v2: 17-4615098-A-G
• gnomAD v3: 17-4711803-A-G
• gnomAD v4: 17-4711803-A-G
• MyVariant Identifiers: chr17:g.4615098A>G (hg19) ; chr17:g.4711803A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4711803A>G , CM000679.2:g.4711803A>G	GRCh38
NC_000017.10:g.4615098A>G , CM000679.1:g.4615098A>G	GRCh37
NC_000017.9:g.4561847A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000269260.7:c.23+1059A>G MANE Select	ENSP00000269260.2:n.23+1059A>G
ENST00000269260.6:c.23+1059A>G	ENSP00000269260.2:n.23+1059A>G
ENST00000346341.6:c.23+1059A>G	ENSP00000341895.2:n.23+1059A>G
ENST00000381488.10:c.23+1059A>G	ENSP00000370898.6:n.23+1059A>G
ENST00000412477.7:c.23+1059A>G	ENSP00000403701.3:n.23+1059A>G
ENST00000570718.5:n.113+1059A>G
ENST00000570739.5:n.113+1059A>G
ENST00000571428.5:c.-478+1059A>G	ENSP00000465877.1:n.-478+1059A>G
ENST00000571791.5:n.63+1059A>G
ENST00000572457.5:c.-462+1059A>G	ENSP00000465296.1:n.-462+1059A>G
ENST00000572497.5:c.23+1059A>G	ENSP00000458946.1:n.23+1059A>G
ENST00000573886.5:n.54+1059A>G
ENST00000574502.5:c.23+1059A>G	ENSP00000458371.1:n.23+1059A>G
ENST00000574888.5:n.90+1059A>G
ENST00000574954.5:c.-523+1059A>G	ENSP00000466344.1:n.-523+1059A>G
ENST00000575131.5:n.84+1059A>G
ENST00000575877.5:c.23+1059A>G	ENSP00000466857.1:n.23+1059A>G
ENST00000576235.1:c.21+1059A>G	ENSP00000460879.1:n.21+1059A>G
NM_001257328.1:c.23+1059A>G	NP_001244257.1:n.23+1059A>G
NM_001257329.1:c.23+1059A>G	NP_001244258.1:n.23+1059A>G
NM_001257330.1:c.23+1059A>G	NP_001244259.1:n.23+1059A>G
NM_001257331.1:c.23+1059A>G	NP_001244260.1:n.23+1059A>G
NM_004313.3:c.23+1059A>G	NP_004304.1:n.23+1059A>G
NM_199004.1:c.23+1059A>G	NP_945355.1:n.23+1059A>G
NR_047516.1:n.251+1059A>G
XM_006721520.1:c.-478+1059A>G	XP_006721583.1:n.-478+1059A>G
XM_011523858.1:c.116+914A>G	XP_011522160.1:n.116+914A>G
XM_011523859.1:c.116+914A>G	XP_011522161.1:n.116+914A>G
NM_001330064.1:c.-478+1059A>G	NP_001316993.1:n.-478+1059A>G
XM_011523858.2:c.116+914A>G	XP_011522160.1:n.116+914A>G
XM_024450751.1:c.23+1059A>G	XP_024306519.1:n.23+1059A>G
XM_024450752.1:c.-523+1059A>G	XP_024306520.1:n.-523+1059A>G
XM_024450753.1:c.-478+1059A>G	XP_024306521.1:n.-478+1059A>G
XR_002958006.1:n.115+1059A>G
XR_002958007.1:n.115+1059A>G
NM_004313.4:c.23+1059A>G MANE Select	NP_004304.1:n.23+1059A>G
NM_001257328.2:c.23+1059A>G	NP_001244257.1:n.23+1059A>G
NM_001257329.2:c.23+1059A>G	NP_001244258.1:n.23+1059A>G
NM_001257330.2:c.23+1059A>G	NP_001244259.1:n.23+1059A>G
NM_001257331.2:c.23+1059A>G	NP_001244260.1:n.23+1059A>G
NM_001330064.2:c.-478+1059A>G	NP_001316993.1:n.-478+1059A>G
NM_199004.2:c.23+1059A>G	NP_945355.1:n.23+1059A>G
NR_047516.2:n.113+1059A>G