Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome 7:76303855 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM086473

Most severe consequence
Clinical significance

Synonyms

LSDB 10825

This variation has 8 HGVS names - click the plus to show

7:g.76303855C>G
ENST00000248553.6:c.418C>G
ENSP00000248553.6:p.Arg140Gly
ENST00000447574.1:c.*582C>G
ENST00000429938.1:c.-87C>G
LRG_248:g.6298C>G
LRG_248t1:c.418C>G
LRG_248p1:p.Arg140Gly

Variation displays