Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 11:47469479 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM080517

Most severe consequence
Clinical significance

Synonyms

LSDB 10273

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

11:g.47469479A>G
ENST00000352508.3:c.416T>C
ENSP00000298853.3:p.Phe139Ser
ENST00000298854.2:c.416T>C
ENSP00000298854.2:p.Phe139Ser
ENST00000529341.1:c.416T>C
ENSP00000431732.1:p.Phe139Ser
ENST00000524487.1:c.416T>C
ENSP00000435551.1:p.Phe139Ser

Variation displays