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
HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 23 sample genotypes.

Variant displays