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 2:240871391 (forward strand) | View in location tab

Co-located

with COSMIC COSM1244655 (G/A) ; HGMD-PUBLIC HM971433

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_000030.2:c.466G>A, 12574

This variation has 5 HGVS names - click the plus to show

2:g.240871391G>A
ENST00000476698.1:n.203G>A
ENST00000472436.1:n.486G>A
ENST00000307503.3:c.466G>A
ENSP00000302620.3:p.Gly156Arg

Variation displays