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 9:108894062 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM030891

Most severe consequence
Clinical significance

Synonyms

LSDB 12149

This variation has 8 HGVS names - click the plus to show

9:g.108894062G>A
ENST00000537196.1:c.1694C>T
ENSP00000439367.1:p.Pro565Leu
ENST00000374647.6:c.2741C>T
ENSP00000363779.5:p.Pro914Leu
LRG_251:g.45267C>T
LRG_251t1.1:c.2741C>T
LRG_251p1.1:p.Pro914Leu

Variation displays