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 11:47447859 (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.47447859C>T
ENST00000352508.5:c.484G>A
ENSP00000298853.3:p.Glu162Lys
ENST00000298854.4:c.484G>A
ENSP00000298854.2:p.Glu162Lys
ENST00000529341.1:c.484G>A
ENSP00000431732.1:p.Glu162Lys
ENST00000524487.3:c.484G>A
ENSP00000435551.2:p.Glu162Lys

Variation displays