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 2:128186136 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM910319

Most severe consequence
Clinical significance

Synonyms

LSDB 17269

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

2:g.128186136G>A
ENST00000409048.1:c.1102G>A
ENSP00000386679.1:p.Gly368Ser
ENST00000402125.2:c.324G>A
ENSP00000384225.2:p.Gly109Ser
ENST00000422777.3:c.1000G>A
ENSP00000409543.3:p.Gly334Ser
ENST00000234071.3:c.1000G>A
ENSP00000234071.3:p.Gly334Ser
ENST00000453608.2:c.1165G>A
ENSP00000404030.2:p.Gly389Ser

Variation displays