Canonical Allele Identifier: CA680251006
Gene: ARRB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.75310457C>G , CM000673.2:g.75310457C>G GRCh38
NC_000011.9:g.75021501C>G , CM000673.1:g.75021501C>G GRCh37
NC_000011.8:g.74699149C>G NCBI36
NG_028118.1:g.46375G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000420843.7:c.21-20418G>C MANE Select ENSP00000409581.2:n.21-20418G>C
ENST00000360025.7:c.21-20418G>C ENSP00000353124.3:n.21-20418G>C
ENST00000420843.6:c.21-20418G>C ENSP00000409581.2:n.21-20418G>C
ENST00000524400.5:c.94+1605G>C
ENST00000533255.1:n.74-20418G>C
ENST00000533609.5:c.63+1605G>C ENSP00000436352.1:n.63+1605G>C
NM_004041.4:c.21-20418G>C NP_004032.2:n.21-20418G>C
NM_020251.3:c.21-20418G>C NP_064647.1:n.21-20418G>C
XM_005273997.1:c.32+1605G>C XP_005274054.1:n.32+1605G>C
XM_011545034.1:c.33-150G>C XP_011543336.1:n.33-150G>C
XM_011545035.1:c.33-150G>C XP_011543337.1:n.33-150G>C
XM_011545034.2:c.33-150G>C XP_011543336.1:n.33-150G>C
XM_011545035.2:c.33-150G>C XP_011543337.1:n.33-150G>C
XM_017017750.1:c.33-150G>C XP_016873239.1:n.33-150G>C
XM_017017751.1:c.33-150G>C XP_016873240.1:n.33-150G>C
XM_017017752.2:c.21-20418G>C XP_016873241.1:n.21-20418G>C
XM_017017754.2:c.21-20418G>C XP_016873243.1:n.21-20418G>C
NM_004041.5:c.21-20418G>C MANE Select NP_004032.2:n.21-20418G>C
NM_020251.4:c.21-20418G>C NP_064647.1:n.21-20418G>C