Original source

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

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

Chromosome 11:17409515 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM051548

Most severe consequence
Evidence status

Clinical significance

This variation has 5 synonyms - click the plus to show

This variation has 7 HGVS names - click the plus to show

11:g.17409515A>G
ENST00000526912.1:c.-17+50T>C
ENST00000528992.1:c.141T>C
ENSP00000436479.1:p.Cys48Arg
ENST00000528731.1:c.-16-122T>C
ENST00000339994.4:c.124T>C
ENSP00000345708.4:p.Cys42Arg

Variation displays