Canonical Allele Identifier: CA2635543346
Gene: ARRB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4710711_4710784del , CM000679.2:g.4710711_4710784del GRCh38
NC_000017.10:g.4614006_4614079del , CM000679.1:g.4614006_4614079del GRCh37
NC_000017.9:g.4560755_4560828del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269260.7:c.-11_23+40del
ENST00000269260.6:c.-11_23+40del
ENST00000346341.6:c.-11_23+40del
ENST00000381488.10:c.-11_23+40del
ENST00000412477.7:c.-11_23+40del
ENST00000570718.5:n.80_113+40del
ENST00000570739.5:n.80_113+40del
ENST00000571428.5:c.-511_-478+40del
ENST00000571791.5:n.30_63+40del
ENST00000572457.5:c.-495_-462+40del
ENST00000572497.5:c.-11_23+40del
ENST00000573886.5:n.21_54+40del
ENST00000574502.5:c.-11_23+40del
ENST00000574888.5:n.57_90+40del
ENST00000574954.5:c.-556_-523+40del
ENST00000575131.5:n.51_84+40del
ENST00000575877.5:c.-11_23+40del
NM_001257328.1:c.-11_23+40del
NM_001257329.1:c.-11_23+40del
NM_001257330.1:c.-11_23+40del
NM_001257331.1:c.-11_23+40del
NM_004313.3:c.-11_23+40del
NM_199004.1:c.-11_23+40del
NR_047516.1:n.218_251+40del
XM_006721520.1:c.-511_-478+40del
NM_001330064.1:c.-511_-478+40del
XM_024450751.1:c.-11_23+40del
XM_024450752.1:c.-556_-523+40del
XM_024450753.1:c.-511_-478+40del
XR_002958006.1:n.82_115+40del
XR_002958007.1:n.82_115+40del
NM_004313.4:c.-11_23+40del
NM_001257328.2:c.-11_23+40del
NM_001257329.2:c.-11_23+40del
NM_001257330.2:c.-11_23+40del
NM_001257331.2:c.-11_23+40del
NM_001330064.2:c.-511_-478+40del
NM_199004.2:c.-11_23+40del
NR_047516.2:n.80_113+40del