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 11:46728138 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM960524

Most severe consequence
Clinical significance

Synonyms

LSDB 4982

This variation has 5 HGVS names - click the plus to show

11:g.46728138C>T
ENST00000530231.3:c.1273C>T
ENSP00000433907.1:p.Arg425Cys
ENST00000311907.7:c.1273C>T
ENSP00000308541.5:p.Arg425Cys

Variation displays