Original source

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

Alleles
-/TA
Location

Chromosome 17: between 41059579 and 41059580 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_000151.2:c.379_380dupTA

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

17:g.41059578_41059579dupTA
ENST00000585489.1:c.379_380dupTA
ENSP00000466202.1:p.Tyr128ThrfsTer3
ENST00000592383.1:c.341-39_341-38dupTA
ENST00000253801.2:c.379_380dupTA
ENSP00000253801.1:p.Tyr128ThrfsTer3
LRG_147:g.11764_11765dupTA
LRG_147t1.1:c.379_380dupTA
LRG_147p1.1:p.Tyr128ThrfsTer3

Variation displays