Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
TGA/-
Location

Chromosome 4:1004391-1004393 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB 6454

This variation has 6 HGVS names - click the plus to show

4:g.1004391_1004393delTGA
ENST00000514224.1:c.1564_1566delTGA
ENSP00000425081.1:p.Ter522delextTer?
ENST00000514698.2:n.2071_2073delTGA
ENST00000247933.5:c.1960_1962delTGA
ENSP00000247933.4:p.Ter654delextTer?

Variation displays