Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 3:183540743 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs7427372

This variation has 5 HGVS names - click the plus to show

3:g.183540743T>C
ENST00000463801.1:n.79+2192A>G
ENST00000431348.1:c.401+2192A>G
ENST00000318631.3:c.401+2192A>G
ENST00000445426.1:c.375+2192A>G

Variation displays