Original source

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

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

Chromosome 4:186066146 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM003619

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_075_SLC25A4_103220_0001, 129

This variation has 5 HGVS names - click the plus to show

4:g.186066146G>C
ENST00000491736.1:c.340G>C
ENSP00000476711.1:p.Ala114Pro
ENST00000281456.6:c.340G>C
ENSP00000281456.5:p.Ala114Pro

Variation displays