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 11:47234872 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM960485

Most severe consequence
Clinical significance

Synonyms

LSDB 9557

This variation has 16 HGVS names - click the plus to show

11:g.47234872G>A
ENST00000617847.3:c.*460G>A
ENST00000256996.7:c.818G>A
ENSP00000256996.3:p.Arg273His
ENST00000616278.3:c.*85+200G>A
ENST00000614394.1:n.208G>A
ENST00000378603.6:c.626G>A
ENSP00000367866.3:p.Arg209His
ENST00000620515.1:n.46+200G>A
ENST00000612309.3:n.1932G>A
ENST00000378601.6:c.702+200G>A
ENST00000378600.6:c.457-2965G>A
ENST00000617022.3:n.1554-2965G>A
LRG_467:g.24931G>A
LRG_467t1:c.818G>A
LRG_467p1:p.Arg273His

About this variant

This variant overlaps 21 transcripts and is associated with 2 phenotypes.

Variation displays