Original source

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

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

Chromosome 11:46739324 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM060261

Most severe consequence
Clinical significance

Synonyms

LSDB 4991

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

11:g.46739324C>G
ENST00000530231.2:c.1668C>G
ENSP00000433907.1:p.Asp556Glu
ENST00000311907.6:c.1785C>G
ENSP00000308541.5:p.Asp595Glu

Variation displays