Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome 2:128186471 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM910320

Most severe consequence
Clinical significance

Synonyms

LSDB 17279

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

2:g.128186471C>G
ENST00000409048.1:c.1437C>G
ENSP00000386679.1:p.Ile479Met
ENST00000402125.2:c.659C>G
ENSP00000384225.2:p.Ile220Met
ENST00000422777.3:c.1335C>G
ENSP00000409543.3:p.Ile445Met
ENST00000453608.2:c.1500C>G
ENSP00000404030.2:p.Ile500Met
ENST00000234071.3:c.1335C>G
ENSP00000234071.3:p.Ile445Met

Variation displays