Canonical Allele Identifier: CA13464484
Gene: ARRB1 HGNC NCBI

Linked Data

dbSNP Id: rs17133858

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.75260513G>T , CM000673.2:g.75260513G>T GRCh38
NC_000011.9:g.74971557G>T , CM000673.1:g.74971557G>T GRCh37
NC_000011.8:g.74649205G>T NCBI36
NG_028118.1:g.96319C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000420843.7:c.*5650C>A MANE Select ENSP00000409581.2:n.*5650C>A
NM_004041.4:c.*5650C>A NP_004032.2:n.*5650C>A
NM_020251.3:c.*5650C>A NP_064647.1:n.*5650C>A
XM_011545034.2:c.*5650C>A XP_011543336.1:n.*5650C>A
XM_011545035.2:c.*5650C>A XP_011543337.1:n.*5650C>A
XM_017017750.1:c.*5650C>A XP_016873239.1:n.*5650C>A
XM_017017751.1:c.*5650C>A XP_016873240.1:n.*5650C>A
XM_017017752.2:c.*5650C>A XP_016873241.1:n.*5650C>A
XM_017017753.1:c.*5650C>A XP_016873242.1:n.*5650C>A
XM_017017754.2:c.*5650C>A XP_016873243.1:n.*5650C>A
NM_004041.5:c.*5650C>A MANE Select NP_004032.2:n.*5650C>A
NM_020251.4:c.*5650C>A NP_064647.1:n.*5650C>A