Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 11:46760891 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM003674

Most severe consequence
Clinical significance

Synonyms

LSDB 4983

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

11:g.46760891G>T
ENST00000530231.1:c.1685G>T
ENSP00000433907.1:p.Gly562Val
ENST00000311907.5:c.1802G>T
ENSP00000308541.5:p.Gly601Val

Variation displays