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 19:17888432 (forward strand) | View in location tab

Co-located

with COSMIC COSM323436 (G/A) ; HGMD-PUBLIC CM981848

Most severe consequence
Clinical significance

Synonyms

LSDB 10651

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

19:g.17888432G>A
ENST00000222248.3:c.1628G>A
ENSP00000222248.2:p.Gly543Glu

Variation displays