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 11:47469411 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM073303

Most severe consequence
Clinical significance

Synonyms

LSDB 10271

This variation has 9 HGVS names - click the plus to show

11:g.47469411C>T
ENST00000352508.3:c.484G>A
ENSP00000298853.3:p.Glu162Lys
ENST00000298854.2:c.484G>A
ENSP00000298854.2:p.Glu162Lys
ENST00000529341.1:c.484G>A
ENSP00000431732.1:p.Glu162Lys
ENST00000524487.1:c.484G>A
ENSP00000435551.1:p.Glu162Lys

Variation displays