Original source

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

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

Chromosome 2:128185950 (forward strand) | View in location tab

Co-located

with COSMIC COSM1006209 (C/T) ; HGMD-PUBLIC CM910317

Most severe consequence
Clinical significance

Synonyms

LSDB 17274

This variation has 11 HGVS names - click the plus to show

2:g.128185950C>T
ENST00000409048.1:c.916C>T
ENSP00000386679.1:p.Arg306Cys
ENST00000402125.2:c.138C>T
ENSP00000384225.2:p.Arg47Cys
ENST00000453608.2:c.979C>T
ENSP00000404030.2:p.Arg327Cys
ENST00000422777.3:c.814C>T
ENSP00000409543.3:p.Arg272Cys
ENST00000234071.3:c.814C>T
ENSP00000234071.3:p.Arg272Cys

Variation displays