Original source

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

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

Chromosome 11:47256859 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM031666

Most severe consequence
Clinical significance

Synonyms

LSDB 9559

This variation has 10 HGVS names - click the plus to show

11:g.47256859G>T
ENST00000378603.3:c.727G>T
ENSP00000367866.3:p.Asp243Tyr
ENST00000378601.3:c.*6G>T
ENST00000378600.3:c.457-2529G>T
ENST00000256996.4:c.919G>T
ENSP00000256996.3:p.Asp307Tyr
LRG_467:g.25367G>T
LRG_467t1.1:c.919G>T
LRG_467p1.1:p.Asp307Tyr

Variation displays