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 19:1398980 (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.1398980C>T
ENST00000447102.5:c.506G>A
ENSP00000403536.2:p.Cys169Tyr
ENST00000591788.2:c.191G>A
ENSP00000466341.2:p.Cys64Tyr
ENST00000252288.4:c.506G>A
ENSP00000252288.1:p.Cys169Tyr

Variation displays