Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 11:64750557 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM981689

Most severe consequence
Clinical significance

Synonyms

LSDB 15731

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

11:g.64750557G>C
ENST00000164139.3:c.1996C>G
ENSP00000164139.3:p.Gln666Glu
ENST00000377432.4:c.1732C>G
ENSP00000366650.3:p.Gln578Glu

Variation displays