Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome 2:241808619 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM910015

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_000030.2:c.198C>G, 12565

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

2:g.241808619C>G
ENST00000472436.1:n.218C>G
ENST00000307503.3:c.198C>G
ENSP00000302620.3:p.Tyr66Ter

Variation displays