Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 2:241808666 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM920011

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 12566, NM_000030.2:c.245G>A

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

2:g.241808666G>A
ENST00000472436.1:n.265G>A
ENST00000307503.3:c.245G>A
ENSP00000302620.3:p.Gly82Glu

Variation displays