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 1:25809096 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB 13654

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

1:g.25809096G>A
ENST00000361547.4:c.818G>A
ENSP00000355141.2:p.Gly273Glu
ENST00000354177.6:c.716G>A
ENSP00000346109.4:p.Gly239Glu
ENST00000374315.1:c.716G>A
ENSP00000363434.1:p.Gly239Glu

Variation displays