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 4:6304014 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM013446

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

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

4:g.6304014G>A
ENST00000507765.1:n.2677G>A
ENST00000503569.1:c.2492G>A
ENSP00000423337.1:p.Gly831Asp
ENST00000226760.1:c.2492G>A
ENSP00000226760.1:p.Gly831Asp

Variation displays