Original source

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

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

Chromosome 19:18786036 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM980431

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

19:g.18786036T>C
ENST00000542601.3:c.1319A>G
ENSP00000439156.2:p.Asp440Gly
ENST00000425807.1:c.1259A>G
ENSP00000403792.1:p.Asp420Gly
ENST00000222271.3:c.1418A>G
ENSP00000222271.2:p.Asp473Gly

Variation displays