Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 13:33017018 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM074308

Most severe consequence
Clinical significance

Synonyms

LSDB 12847

This variation has 4 HGVS names - click the plus to show

13:g.33017018A>G
ENST00000380099.3:c.578A>G
ENSP00000369442.3:p.His193Arg
ENST00000487852.1:n.586A>G

Variation displays