Original source

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

Alleles
ATA/-
Location

Chromosome 5:37001030-37001032 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB 15883

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

5:g.37001030_37001032delATA
ENST00000448238.2:c.3616_3618delATA
ENSP00000406266.2:p.Ile1206del
ENST00000282516.10:c.3616_3618delATA
ENSP00000282516.8:p.Ile1206del
ENST00000621733.1:c.1-63548_1-63546delATA

Variation displays