Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 9:32984799 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB 13720

This variation has 42 HGVS names - click the plus to show

9:g.32984799T>C
ENST00000485479.3:c.*332A>G
ENST00000480031.3:c.*396A>G
ENST00000479656.3:c.*447A>G
ENST00000379813.5:c.584A>G
ENSP00000369141.4:p.His195Arg
ENST00000463596.3:c.602A>G
ENSP00000419846.1:p.His201Arg
ENST00000397172.5:c.428A>G
ENSP00000380357.3:p.His143Arg
ENST00000465003.3:c.*229A>G
ENST00000309615.5:c.440A>G
ENSP00000311547.4:p.His147Arg
ENST00000478279.3:c.*229A>G
ENST00000464632.3:c.*332A>G
ENST00000379812.7:c.428A>G
ENSP00000369140.5:p.His143Arg
ENST00000379825.4:c.644A>G
ENSP00000369153.2:p.His215Arg
ENST00000482687.3:c.543+1172A>G
ENST00000473221.3:c.482A>G
ENSP00000419020.1:p.His161Arg
ENST00000495360.3:c.*332A>G
ENST00000486724.3:n.338A>G
ENST00000477119.1:c.440A>G
ENSP00000417649.1:p.His147Arg
ENST00000436040.4:c.602A>G
ENSP00000400806.3:p.His201Arg
ENST00000494649.3:c.*447A>G
ENST00000476858.3:c.482A>G
ENSP00000419042.1:p.His161Arg
ENST00000467331.3:c.*447A>G
ENST00000379817.4:c.602A>G
ENSP00000369145.2:p.His201Arg
ENST00000460940.3:c.*388+1172A>G
ENST00000474658.4:c.*45A>G
ENST00000379819.3:c.644A>G
ENSP00000369147.1:p.His215Arg
ENST00000483148.3:c.*170+1172A>G
ENST00000472896.3:c.*273+1172A>G
ENST00000468275.3:c.602A>G
ENSP00000420263.1:p.His201Arg

Variation displays