Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M
Location

Chromosome 19:17877840 (forward strand) | View in location tab

Co-located

with COSMIC COSM1480779 (C/T) ; HGMD-PUBLIC CM971392

Most severe consequence
Clinical significance

Synonyms

LSDB 10647

This variation has 3 HGVS names - click the plus to show

19:g.17877840C>A
ENST00000222248.3:c.816C>A
ENSP00000222248.2:p.Cys272Ter

Variation displays