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 | MAF: 0.13 (T)
Location

Chromosome 5:96783162 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_021556

This variation has 6 HGVS names - click the plus to show

5:g.96783162C>T
ENST00000443439.3:c.2174G>A
ENSP00000406304.2:p.Arg725Gln
ENST00000514604.2:n.598G>A
ENST00000296754.4:c.2174G>A
ENSP00000296754.3:p.Arg725Gln

This variation has assays on 5 chips - click the plus to show

Variation displays