Canonical Allele Identifier: CA13464484
Gene: ARRB1 HGNC NCBI
MyVariant.info:
GRCh38 chr11:g.75260513G>T
GRCh37 chr11:g.74971557G>T
gnomAD v2:
11:74971557 G / T
gnomAD v3:
11:75260513 G / T
gnomAD v4:
chr11-75260513-G-T
Joint Max Group AF 0.14081308 (AFR)
Genomes Max Group AF 0.14081308 (AFR)
Exomes Max Group AF 0.01460131 (NFE)
dbSNP:
17133858
JSON-LD

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
Search 100 bp 5'
Search 100 bp 3'