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 18:58128734 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 15 HGVS names - click the plus to show

18:g.58128734C>T
ENST00000590694.3:n.92-37054C>T
ENST00000591579.3:n.93-37054C>T
ENST00000585594.3:n.169-37054C>T
ENST00000591989.3:n.101-37058C>T
ENST00000356462.8:c.49-37054C>T
ENST00000592846.3:c.-370-37058C>T
ENST00000588516.3:n.1149-37054C>T
ENST00000589054.3:c.48+84026C>T
ENST00000400345.5:c.49-37054C>T
ENST00000256830.11:c.49-37054C>T
ENST00000585363.3:n.86-37054C>T
ENST00000382850.6:c.49-37054C>T
ENST00000587547.1:n.838-37054C>T
ENST00000456986.3:c.-315-37054C>T

Variation displays