Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 11:17387934 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM102333, CM045416

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

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

11:g.17387934C>T
ENST00000528992.1:c.175G>A
ENSP00000436479.1:p.Gly59Asp
ENST00000526912.1:c.-17+84G>A
ENST00000528731.1:c.-16-88G>A
ENST00000339994.4:c.158G>A
ENSP00000345708.4:p.Gly53Asp

Variation displays