Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.02 (G)
Location

Chromosome 19:41353871 (forward strand) | View in location tab

Most severe consequence
Evidence status

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

19:g.41353871C>G
ENST00000221930.5:c.-827G>C
ENST00000604424.1:n.350+2669C>G
ENST00000539627.3:c.-30+2669C>G

Variation displays