Original source

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

Alleles
-/TA
Location

Chromosome 17: between 42907562 and 42907563 (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.42907561_42907562dupTA
ENST00000585489.1:c.379_380dupTA
ENSP00000466202.1:p.Tyr128ThrfsTer3
ENST00000253801.4:c.379_380dupTA
ENSP00000253801.1:p.Tyr128ThrfsTer3
ENST00000592383.3:c.341-39_341-38dupTA
LRG_147:g.11764_11765dupTA
LRG_147t1:c.379_380dupTA
LRG_147p1:p.Tyr128ThrfsTer3

Variation displays