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 1:45014835 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM920703, CD962174

Most severe consequence
Clinical significance

Synonyms

LSDB 4802

This variation has 7 HGVS names - click the plus to show

1:g.45014835C>G
ENST00000472254.1:n.627C>G
ENST00000466193.1:n.297C>G
ENST00000465678.1:n.289C>G
ENST00000494399.2:n.1541C>G
ENST00000246337.5:c.874C>G
ENSP00000246337.4:p.Arg292Gly

Variation displays