Original source

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

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

Chromosome 11:64752064 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM930631

Most severe consequence
Clinical significance

Synonyms

LSDB 15724

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

11:g.64752064T>G
ENST00000164139.3:c.1628A>C
ENSP00000164139.3:p.Lys543Thr
ENST00000377432.4:c.1364A>C
ENSP00000366650.3:p.Lys455Thr

Variation displays