Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 11:46726734 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM000010

Most severe consequence
Clinical significance

Synonyms

LSDB 4988

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

11:g.46726734G>A
ENST00000530231.2:c.1027G>A
ENSP00000433907.1:p.Glu343Lys
ENST00000311907.6:c.1027G>A
ENSP00000308541.5:p.Glu343Lys

Variation displays