Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.28 (G)
Location

Chromosome 15:77671545 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59418404

This variation has 10 HGVS names - click the plus to show

15:g.77671545A>G
ENST00000570216.2:c.-13+5544T>C
ENST00000559893.2:c.-13+5544T>C
ENST00000562933.2:c.-13+5544T>C
ENST00000563316.2:c.-13+5544T>C
ENST00000567726.2:c.-13+5544T>C
ENST00000561030.2:c.-13+5544T>C
ENST00000566711.2:c.-13+5544T>C
ENST00000561686.2:c.-13+19175T>C
ENST00000564472.2:c.-13+5544T>C

This variation has assays on 11 chips - click the plus to show

Variation displays