Original source

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

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

Chromosome 4:6301739 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM982041

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 13626, 2010_April_001_086_WFS1_606201_0005

This variation has 6 HGVS names - click the plus to show

4:g.6301739G>A
ENST00000507765.1:n.2129G>A
ENST00000503569.2:c.1944G>A
ENSP00000423337.1:p.Trp648Ter
ENST00000226760.2:c.1944G>A
ENSP00000226760.1:p.Trp648Ter

Variation displays