Canonical Allele Identifier: CA980945345
Gene: ARRB2 HGNC NCBI

Linked Data

dbSNP Id: rs1053051945
gnomAD v3: 17-4710662-G-T
gnomAD v4: 17-4710662-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4710662G>T , CM000679.2:g.4710662G>T GRCh38
NC_000017.10:g.4613957G>T , CM000679.1:g.4613957G>T GRCh37
NC_000017.9:g.4560706G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269260.7:c.-60G>T MANE Select ENSP00000269260.2:n.-60G>T
ENST00000269260.6:c.-60G>T ENSP00000269260.2:n.-60G>T
ENST00000346341.6:c.-60G>T ENSP00000341895.2:n.-60G>T
ENST00000570718.5:n.31G>T
ENST00000570739.5:n.31G>T
ENST00000572457.5:c.-544G>T ENSP00000465296.1:n.-544G>T
ENST00000574502.5:c.-60G>T ENSP00000458371.1:n.-60G>T
ENST00000574888.5:n.8G>T
ENST00000574954.5:c.-605G>T ENSP00000466344.1:n.-605G>T
ENST00000575131.5:n.2G>T
NM_001257328.1:c.-60G>T NP_001244257.1:n.-60G>T
NM_001257329.1:c.-60G>T NP_001244258.1:n.-60G>T
NM_001257330.1:c.-60G>T NP_001244259.1:n.-60G>T
NM_001257331.1:c.-60G>T NP_001244260.1:n.-60G>T
NM_004313.3:c.-60G>T NP_004304.1:n.-60G>T
NM_199004.1:c.-60G>T NP_945355.1:n.-60G>T
NR_047516.1:n.169G>T
XM_006721520.1:c.-560G>T XP_006721583.1:n.-560G>T
NM_001330064.1:c.-560G>T NP_001316993.1:n.-560G>T
XM_024450751.1:c.-60G>T XP_024306519.1:n.-60G>T
XM_024450752.1:c.-605G>T XP_024306520.1:n.-605G>T
XM_024450753.1:c.-560G>T XP_024306521.1:n.-560G>T
XR_002958006.1:n.33G>T
XR_002958007.1:n.33G>T
NM_004313.4:c.-60G>T MANE Select NP_004304.1:n.-60G>T
NM_001257328.2:c.-60G>T NP_001244257.1:n.-60G>T
NM_001257329.2:c.-60G>T NP_001244258.1:n.-60G>T
NM_001257330.2:c.-60G>T NP_001244259.1:n.-60G>T
NM_001257331.2:c.-60G>T NP_001244260.1:n.-60G>T
NM_001330064.2:c.-560G>T NP_001316993.1:n.-560G>T
NM_199004.2:c.-60G>T NP_945355.1:n.-60G>T
NR_047516.2:n.31G>T