Original source

Variation features from DPGP, with Ensembl identifiers (release 1) | DPGP 1

Alleles
G/A/C/T | Ambiguity code: N
Location

Chromosome 2L:1056714 (forward strand) | View in location tab

Most severe consequence
 
Intron variant

This variant has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts and has 23 sample genotypes.

Variant displays