Most severe consequence
24
upstream gene variant
Alleles
C/T
Note: The reference base for this variant (C) does not match the Ensembl reference base (G) at this location.
Note: The reference base for this variant (C) does not match the Ensembl reference base (G) at this location.
Location
Chromosome 1:19731 (forward strand)|VCF:1 19731 rs5413863126 C T
HGVS name
1:g.19731G>T
External Links
Original source
EVA2024_rsID_mapped
About this variant
This variant overlaps 2 transcripts.
