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 16:86567697 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM021601

Most severe consequence
Clinical significance

Synonyms

LSDB 11048

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

16:g.86567697G>A
ENST00000320354.5:c.362G>A
ENSP00000326371.4:p.Arg121His
ENST00000563280.1:n.65C>T

Variation displays