Original source

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

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

Chromosome 11:64751331 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM951095

Most severe consequence
Clinical significance

Synonyms

LSDB 15726

This variation has 6 HGVS names - click the plus to show

11:g.64751331C>T
ENST00000164139.3:c.1963G>A
ENSP00000164139.3:p.Glu655Lys
ENST00000462303.1:n.287G>A
ENST00000377432.4:c.1699G>A
ENSP00000366650.3:p.Glu567Lys

Variation displays