Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 9:91724229 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM000567

Most severe consequence
Clinical significance

Synonyms

LSDB 10983

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

9:g.91724229G>T
ENST00000550066.3:n.2733C>A
ENST00000375715.3:c.1845C>A
ENSP00000364867.1:p.Tyr615Ter
ENST00000375708.3:c.2265C>A
ENSP00000364860.3:p.Tyr755Ter

Variation displays