Original source

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

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

Chromosome 11:47256335 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CD031829, CM960484

Most severe consequence
Clinical significance

Synonyms

LSDB 9556

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

11:g.47256335A>G
ENST00000378603.3:c.538A>G
ENSP00000367866.3:p.Lys180Glu
ENST00000378601.3:c.702+112A>G
ENST00000378600.3:c.457-3053A>G
ENST00000256996.4:c.730A>G
ENSP00000256996.3:p.Lys244Glu
LRG_467:g.24843A>G
LRG_467t1.1:c.730A>G
LRG_467p1.1:p.Lys244Glu

Variation displays