Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 12:32955433 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM043061

Most severe consequence
Clinical significance

Synonyms

LSDB 11518

This variation has 6 HGVS names - click the plus to show

12:g.32955433G>A
ENST00000340811.4:c.2071C>T
ENSP00000342800.4:p.Arg691Ter
ENST00000070846.6:c.2203C>T
ENSP00000070846.6:p.Arg735Ter
ENST00000549461.1:n.517C>T

Variation displays