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 20:34292467 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM045450

Most severe consequence
Clinical significance

Synonyms

LSDB 5340

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

20:g.34292467C>T
ENST00000468908.1:n.499G>A
ENST00000217426.4:c.336G>A
ENSP00000217426.2:p.Trp112Ter
ENST00000538132.1:c.252G>A
ENSP00000442820.1:p.Trp84Ter
ENST00000480653.3:n.383G>A

Variation displays