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 17:42904028 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM972910, CM960669

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_055_G6PC_232200_0009, 6322

This variation has 11 HGVS names - click the plus to show

17:g.42904028G>A
ENST00000585489.1:c.328G>A
ENSP00000466202.1:p.Glu110Lys
ENST00000588481.1:n.393G>A
ENST00000253801.4:c.328G>A
ENSP00000253801.1:p.Glu110Lys
ENST00000592383.3:c.328G>A
ENSP00000465958.1:p.Glu110Lys
LRG_147:g.8231G>A
LRG_147t1.1:c.328G>A
LRG_147p1.1:p.Glu110Lys

Variation displays