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 11:17461767 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM067629

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 8 HGVS names - click the plus to show

11:g.17461767A>C
ENST00000389817.4:c.638T>G
ENSP00000374467.3:p.Leu213Arg
ENST00000527905.2:c.638T>G
ENSP00000431653.1:p.Leu213Arg
ENST00000532728.2:n.669T>G
ENST00000302539.5:c.638T>G
ENSP00000303960.4:p.Leu213Arg

Variation displays