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 11:44135774 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM970452

Most severe consequence
Clinical significance

Synonyms

LSDB 15579

This variation has 10 HGVS names - click the plus to show

11:g.44135774C>G
ENST00000533608.1:c.666C>G
ENSP00000431173.1:p.Tyr222Ter
ENST00000358681.4:c.666C>G
ENSP00000351509.4:p.Tyr222Ter
ENST00000529186.1:n.364C>G
ENST00000395673.3:c.765C>G
ENSP00000379032.3:p.Tyr255Ter
ENST00000343631.3:c.666C>G
ENSP00000342656.3:p.Tyr222Ter

Variation displays