Original source

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

Alleles
G/T | Ancestral: T | Ambiguity code: K | MAF: 0.45 (G)
Location

Chromosome 19:42265889 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 5 synonyms - click the plus to show

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

19:g.42265889G>T
ENST00000601409.1:n.384-3900C>A
ENST00000199764.6:c.716G>T
ENSP00000199764.6:p.Gly239Val

This variation has assays on 4 chips - click the plus to show

Variation displays