Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/G|Ancestral: C|Ambiguity code: S|MAF: 0.01 (G)
Location

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

Most severe consequence
 
5 prime UTR variant
Evidence status

HGVS names

This variant has 4 HGVS names - Hide

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

About this variant

This variant overlaps 6 transcripts, 2 regulatory features, has 2548 sample genotypes and is mentioned in 1 citation.

Variant displays