Canonical Allele Identifier: CA397264888
Gene: ARRB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4719346C>G , CM000679.2:g.4719346C>G GRCh38
NC_000017.10:g.4622641C>G , CM000679.1:g.4622641C>G GRCh37
NC_000017.9:g.4569390C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269260.7:c.843C>G MANE Select ENSP00000269260.2:p.Asp281Glu
ENST00000269260.6:c.843C>G ENSP00000269260.2:p.Asp281Glu
ENST00000346341.6:c.798C>G ENSP00000341895.2:p.Asp266Glu
ENST00000381488.10:c.798C>G ENSP00000370898.6:p.Asp266Glu
ENST00000412477.7:c.906C>G ENSP00000403701.3:p.Asp302Glu
ENST00000571206.1:c.267C>G ENSP00000460607.1:p.Asp89Glu
ENST00000571428.5:c.267C>G ENSP00000465877.1:p.Asp89Glu
ENST00000572457.5:c.267C>G ENSP00000465296.1:p.Asp89Glu
ENST00000574502.5:c.*321C>G ENSP00000458371.1:n.*321C>G
ENST00000574954.5:c.267C>G ENSP00000466344.1:p.Asp89Glu
ENST00000575877.5:c.786+57C>G ENSP00000466857.1:n.786+57C>G
ENST00000576235.1:c.725C>G ENSP00000460879.1:n.725C>G
NM_001257328.1:c.906C>G NP_001244257.1:p.Asp302Glu
NM_001257329.1:c.786+57C>G NP_001244258.1:n.786+57C>G
NM_001257330.1:c.843C>G NP_001244259.1:p.Asp281Glu
NM_001257331.1:c.798C>G NP_001244260.1:p.Asp266Glu
NM_004313.3:c.843C>G NP_004304.1:p.Asp281Glu
NM_199004.1:c.798C>G NP_945355.1:p.Asp266Glu
NR_047516.1:n.1040C>G
XM_006721520.1:c.267C>G XP_006721583.1:p.Asp89Glu
XM_006721521.1:c.267C>G XP_006721584.1:p.Asp89Glu
XM_011523858.1:c.936C>G XP_011522160.1:p.Asp312Glu
XM_011523859.1:c.891C>G XP_011522161.1:p.Asp297Glu
NM_001330064.1:c.267C>G NP_001316993.1:p.Asp89Glu
XM_011523858.2:c.936C>G XP_011522160.1:p.Asp312Glu
XM_017024645.1:c.267C>G XP_016880134.1:p.Asp89Glu
XM_024450751.1:c.843C>G XP_024306519.1:p.Asp281Glu
XM_024450752.1:c.267C>G XP_024306520.1:p.Asp89Glu
XM_024450753.1:c.267C>G XP_024306521.1:p.Asp89Glu
XR_002958006.1:n.850C>G
XR_002958007.1:n.850C>G
NM_004313.4:c.843C>G MANE Select NP_004304.1:p.Asp281Glu
NM_001257328.2:c.906C>G NP_001244257.1:p.Asp302Glu
NM_001257329.2:c.786+57C>G NP_001244258.1:n.786+57C>G
NM_001257330.2:c.843C>G NP_001244259.1:p.Asp281Glu
NM_001257331.2:c.798C>G NP_001244260.1:p.Asp266Glu
NM_001330064.2:c.267C>G NP_001316993.1:p.Asp89Glu
NM_199004.2:c.798C>G NP_945355.1:p.Asp266Glu
NR_047516.2:n.902C>G