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 2:15945883 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM056657

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_092_MYCN_164840_0003, 4417

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

2:g.15945883G>A
ENST00000281043.3:c.1181G>A
ENSP00000281043.3:p.Arg394His

Variation displays