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 7:94427654 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM070850

Most severe consequence
Clinical significance

Synonyms

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

7:g.94427654G>A
ENST00000481570.2:n.4076G>A
ENST00000297268.7:c.3295G>A
ENSP00000297268.6:p.Gly1099Arg
ENST00000620463.1:c.3289G>A
ENSP00000477719.1:p.Gly1097Arg
ENST00000464916.1:n.343G>A
LRG_2:g.38094G>A
LRG_2t1.1:c.3295G>A
LRG_2p1.1:p.Gly1099Arg

Variation displays