Original source

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

Alleles
CTT/-
Location

Chromosome 3:197951229-197951231 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB NM_000996.2:c.82_84delCTT

This variation has 17 HGVS names - click the plus to show

3:g.197951229_197951231delCTT
ENST00000265239.8:c.-59-5545_-59-5543delAAG
ENST00000439255.1:c.82_84delCTT
ENSP00000410683.1:p.Leu28del
ENST00000480302.3:n.313-5545_313-5543delAAG
ENST00000496582.3:n.143_145delCTT
ENST00000464167.3:c.82_84delCTT
ENSP00000419117.1:p.Leu28del
ENST00000448864.3:c.82_84delCTT
ENSP00000393393.1:p.Leu28del
ENST00000485439.3:n.146_148delCTT
ENST00000442341.3:c.82_84delCTT
ENSP00000387688.1:p.Leu28del
ENST00000329092.10:n.143_145delCTT
ENST00000429437.3:c.82_84delCTT
ENSP00000398058.1:p.Leu28del
ENST00000416896.1:c.-49-7180_-49-7178delAAG

Variation displays