Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 2:128186038 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM910318

Most severe consequence
Clinical significance

Synonyms

LSDB 17263

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

2:g.128186038C>T
ENST00000409048.1:c.1004C>T
ENSP00000386679.1:p.Ala335Val
ENST00000402125.2:c.226C>T
ENSP00000384225.2:p.Ala76Val
ENST00000453608.2:c.1067C>T
ENSP00000404030.2:p.Ala356Val
ENST00000422777.3:c.902C>T
ENSP00000409543.3:p.Ala301Val
ENST00000234071.3:c.902C>T
ENSP00000234071.3:p.Ala301Val

Variation displays