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: 0.37 (T)
Location

Chromosome 20:63712604 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 11 HGVS names - click the plus to show

20:g.63712604T>G
ENST00000448100.3:c.584+3440T>G
ENST00000477340.2:n.692+3440T>G
ENST00000328969.5:c.584+3440T>G
ENST00000357119.5:c.584+3440T>G
ENST00000478385.2:n.167+3440T>G
ENST00000490623.2:c.301+3440T>G
ENST00000355969.7:c.584+3440T>G
ENST00000472711.2:n.284+3440T>G
ENST00000369967.4:c.584+3440T>G
ENST00000468235.1:n.76+3440T>G

This variation has assays on 10 chips - click the plus to show

Variation displays