Original source

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

Alleles
C/- | Ancestral: C | MAF: 0.45 (-)
Location

Chromosome 11:102670496 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 8 HGVS names - click the plus to show

HG305_PATCH:g.102670496delC
ENST00000572001.1:n.443+1643delC
ENST00000572697.1:n.682+1643delC
11:g.102670496delC
ENST00000525739.2:n.682+1643delC
ENST00000371455.3:n.423+1643delC
ENST00000575579.1:n.423+1643delC
ENST00000544704.1:n.443+1643delC

Variation displays