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 2:127428560 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM910319

Most severe consequence
Clinical significance

Synonyms

LSDB 17269

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

2:g.127428560G>A
ENST00000402125.2:c.324G>A
ENSP00000384225.2:p.Gly109Ser
ENST00000409048.1:c.1102G>A
ENSP00000386679.1:p.Gly368Ser
ENST00000234071.5:c.1000G>A
ENSP00000234071.3:p.Gly334Ser

Variation displays