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 13:110186513 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB NM_001845.4:c.1769G>A

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

13:g.110186513C>T
ENST00000375820.5:c.1769G>A
ENSP00000364979.4:p.Gly590Glu

Variation displays