Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 11:17409603 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM970815

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 9658, 2010_April_001_202_KCNJ11_600937_0009

This variation has 7 HGVS names - click the plus to show

11:g.17409603G>T
ENST00000526912.1:c.-55C>A
ENST00000528992.1:c.53C>A
ENSP00000436479.1:p.Tyr18Ter
ENST00000528731.1:c.-16-210C>A
ENST00000339994.4:c.36C>A
ENSP00000345708.4:p.Tyr12Ter

Variation displays