Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 9:91737400 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM002099

Most severe consequence
Clinical significance

Synonyms

LSDB 10989

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

9:g.91737400G>A
ENST00000550066.2:n.1081C>T
ENST00000375715.2:c.193C>T
ENSP00000364867.1:p.Arg65Ter
ENST00000375708.3:c.613C>T
ENSP00000364860.3:p.Arg205Ter

Variation displays