Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 11:124868837 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM041425

Most severe consequence
Clinical significance

Synonyms

LSDB 15856

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

11:g.124868837A>C
ENST00000397801.2:c.196A>C
ENSP00000380903.1:p.Ile66Leu
ENST00000538940.2:c.130A>C
ENSP00000441797.1:p.Ile44Leu

Variation displays