Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 9:32984797 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB 13720

This variation has 41 HGVS names - click the plus to show

9:g.32984797T>C
ENST00000485479.1:c.*332A>G
ENST00000480031.1:c.*396A>G
ENST00000479656.1:c.*447A>G
ENST00000379813.3:c.602A>G
ENSP00000369141.3:p.His201Arg
ENST00000397172.3:c.428A>G
ENSP00000380357.3:p.His143Arg
ENST00000463596.1:c.602A>G
ENSP00000419846.1:p.His201Arg
ENST00000465003.1:c.*229A>G
ENST00000309615.3:c.644A>G
ENSP00000311547.3:p.His215Arg
ENST00000478279.1:c.*229A>G
ENST00000379812.5:c.428A>G
ENSP00000369140.5:p.His143Arg
ENST00000464632.1:c.*332A>G
ENST00000379825.2:c.644A>G
ENSP00000369153.2:p.His215Arg
ENST00000482687.1:c.543+1172A>G
ENST00000473221.1:c.482A>G
ENSP00000419020.1:p.His161Arg
ENST00000495360.1:c.*332A>G
ENST00000486724.1:n.338A>G
ENST00000477119.1:c.440A>G
ENSP00000417649.1:p.His147Arg
ENST00000436040.2:c.543+1172A>G
ENST00000494649.1:c.*447A>G
ENST00000476858.1:c.482A>G
ENSP00000419042.1:p.His161Arg
ENST00000467331.1:c.*447A>G
ENST00000379817.2:c.602A>G
ENSP00000369145.2:p.His201Arg
ENST00000460940.1:c.*388+1172A>G
ENST00000474658.2:c.*45A>G
ENST00000379819.1:c.644A>G
ENSP00000369147.1:p.His215Arg
ENST00000483148.1:c.*170+1172A>G
ENST00000468275.1:c.602A>G
ENSP00000420263.1:p.His201Arg
ENST00000472896.1:c.*273+1172A>G

Variation displays