Original source

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

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

Chromosome 19:1398979 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM057970

Most severe consequence
Clinical significance

Synonyms

LSDB 10025

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

19:g.1398979C>T
ENST00000447102.3:c.506G>A
ENSP00000403536.2:p.Cys169Tyr
ENST00000591788.1:c.183G>A
ENSP00000466341.1:p.Cys62Tyr
ENST00000252288.2:c.506G>A
ENSP00000252288.1:p.Cys169Tyr

Variation displays