Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

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

Chromosome 20:46726312 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM080547

Most severe consequence
Clinical significance

Synonyms

LSDB 13567

This variation has 3 HGVS names - click the plus to show

20:g.46726312G>T
ENST00000359271.3:c.1276G>T
ENSP00000352216.2:p.Gly426Trp

Variation displays