Original source

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

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

Chromosome 19:41761981 (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.41761981T>G
ENST00000601409.1:n.384-3900A>C
ENST00000199764.6:c.716T>G
ENSP00000199764.6:p.Val239Gly

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

Variation displays