Original source

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

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

Chromosome 11:47464332 (forward strand) | View in location tab

Co-located

with COSMIC COSM542642 (G/A) ; HGMD-PUBLIC CM080516

Most severe consequence
Clinical significance

Synonyms

LSDB 10274

This variation has 8 HGVS names - click the plus to show

11:g.47464332G>A
ENST00000352508.3:c.566C>T
ENSP00000298853.3:p.Ala189Val
ENST00000298854.2:c.566C>T
ENSP00000298854.2:p.Ala189Val
ENST00000529341.1:c.566C>T
ENSP00000431732.1:p.Ala189Val
ENST00000524487.1:c.532-859C>T

Variation displays