Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 2:128186163 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM920596

Most severe consequence
Clinical significance

Synonyms

LSDB 17266

This variation has 11 HGVS names - click the plus to show

2:g.128186163G>A
ENST00000409048.1:c.1129G>A
ENSP00000386679.1:p.Gly377Ser
ENST00000402125.2:c.351G>A
ENSP00000384225.2:p.Gly118Ser
ENST00000453608.2:c.1192G>A
ENSP00000404030.2:p.Gly398Ser
ENST00000422777.3:c.1027G>A
ENSP00000409543.3:p.Gly343Ser
ENST00000234071.3:c.1027G>A
ENSP00000234071.3:p.Gly343Ser

Variation displays