Canonical Allele Identifier: CA397264883

Gene: ARRB2

Linked Data

• gnomAD v4: 17-4719344-G-T
• MyVariant Identifiers: chr17:g.4622639G>T (hg19) ; chr17:g.4719344G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4719344G>T , CM000679.2:g.4719344G>T	GRCh38
NC_000017.10:g.4622639G>T , CM000679.1:g.4622639G>T	GRCh37
NC_000017.9:g.4569388G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269260.7:c.841G>T MANE Select	ENSP00000269260.2:p.Asp281Tyr
ENST00000269260.6:c.841G>T	ENSP00000269260.2:p.Asp281Tyr
ENST00000346341.6:c.796G>T	ENSP00000341895.2:p.Asp266Tyr
ENST00000381488.10:c.796G>T	ENSP00000370898.6:p.Asp266Tyr
ENST00000412477.7:c.904G>T	ENSP00000403701.3:p.Asp302Tyr
ENST00000571206.1:c.265G>T	ENSP00000460607.1:p.Asp89Tyr
ENST00000571428.5:c.265G>T	ENSP00000465877.1:p.Asp89Tyr
ENST00000572457.5:c.265G>T	ENSP00000465296.1:p.Asp89Tyr
ENST00000574502.5:c.*319G>T	ENSP00000458371.1:n.*319G>T
ENST00000574954.5:c.265G>T	ENSP00000466344.1:p.Asp89Tyr
ENST00000575877.5:c.786+55G>T	ENSP00000466857.1:n.786+55G>T
ENST00000576235.1:c.723G>T	ENSP00000460879.1:n.723G>T
NM_001257328.1:c.904G>T	NP_001244257.1:p.Asp302Tyr
NM_001257329.1:c.786+55G>T	NP_001244258.1:n.786+55G>T
NM_001257330.1:c.841G>T	NP_001244259.1:p.Asp281Tyr
NM_001257331.1:c.796G>T	NP_001244260.1:p.Asp266Tyr
NM_004313.3:c.841G>T	NP_004304.1:p.Asp281Tyr
NM_199004.1:c.796G>T	NP_945355.1:p.Asp266Tyr
NR_047516.1:n.1038G>T
XM_006721520.1:c.265G>T	XP_006721583.1:p.Asp89Tyr
XM_006721521.1:c.265G>T	XP_006721584.1:p.Asp89Tyr
XM_011523858.1:c.934G>T	XP_011522160.1:p.Asp312Tyr
XM_011523859.1:c.889G>T	XP_011522161.1:p.Asp297Tyr
NM_001330064.1:c.265G>T	NP_001316993.1:p.Asp89Tyr
XM_011523858.2:c.934G>T	XP_011522160.1:p.Asp312Tyr
XM_017024645.1:c.265G>T	XP_016880134.1:p.Asp89Tyr
XM_024450751.1:c.841G>T	XP_024306519.1:p.Asp281Tyr
XM_024450752.1:c.265G>T	XP_024306520.1:p.Asp89Tyr
XM_024450753.1:c.265G>T	XP_024306521.1:p.Asp89Tyr
XR_002958006.1:n.848G>T
XR_002958007.1:n.848G>T
NM_004313.4:c.841G>T MANE Select	NP_004304.1:p.Asp281Tyr
NM_001257328.2:c.904G>T	NP_001244257.1:p.Asp302Tyr
NM_001257329.2:c.786+55G>T	NP_001244258.1:n.786+55G>T
NM_001257330.2:c.841G>T	NP_001244259.1:p.Asp281Tyr
NM_001257331.2:c.796G>T	NP_001244260.1:p.Asp266Tyr
NM_001330064.2:c.265G>T	NP_001316993.1:p.Asp89Tyr
NM_199004.2:c.796G>T	NP_945355.1:p.Asp266Tyr
NR_047516.2:n.900G>T