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 11:124871062 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM041427

Most severe consequence
Clinical significance

Synonyms

LSDB 15848

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

11:g.124871062G>A
ENST00000538940.2:c.1016G>A
ENSP00000441797.1:p.Gly339Glu
ENST00000397801.2:c.1082G>A
ENSP00000380903.1:p.Gly361Glu

Variation displays