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 13:110187311 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM076123

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 962, NM_001845.4:c.1555G>A

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

13:g.110187311C>T
ENST00000375820.6:c.1555G>A
ENSP00000364979.4:p.Gly519Arg

Variation displays