Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 11:17387316 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM053288

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 9662, 2010_April_001_205_KCNJ11_600937_0013

This variation has 5 HGVS names - click the plus to show

11:g.17387316T>C
ENST00000528731.1:c.515A>G
ENSP00000434755.1:p.His172Arg
ENST00000339994.4:c.776A>G
ENSP00000345708.4:p.His259Arg

Variation displays