Original source

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

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

Chromosome 12:21642032 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM990786, CM900151

Most severe consequence
Clinical significance

Synonyms

LSDB 3770

This variation has 7 HGVS names - click the plus to show

12:g.21642032C>T
ENST00000396076.3:c.515G>A
ENSP00000379386.1:p.Arg172His
ENST00000350669.3:c.515G>A
ENSP00000229319.1:p.Arg172His
ENST00000396075.3:c.515G>A
ENSP00000379385.1:p.Arg172His

Variation displays