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 19:17882160 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM991141

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 10652

This variation has 4 HGVS names - click the plus to show

19:g.17882160G>A
ENST00000597109.1:n.182G>A
ENST00000222248.3:c.1183G>A
ENSP00000222248.2:p.Gly395Arg

Variation displays