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 2:240868986 (forward strand) | View in location tab

Co-located

with COSMIC COSM308997 (G/-) ; HGMD-PUBLIC CM930013

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 12567, NM_000030.2:c.121G>A

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

2:g.240868986G>A
ENST00000472436.1:n.141G>A
ENST00000307503.3:c.121G>A
ENSP00000302620.3:p.Gly41Arg

Variation displays