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 11:124870650 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM041426

Most severe consequence
Clinical significance

Synonyms

LSDB 15853

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

11:g.124870650G>A
ENST00000397801.3:c.955G>A
ENSP00000380903.1:p.Glu319Lys
ENST00000538940.3:c.889G>A
ENSP00000441797.1:p.Glu297Lys

Variation displays